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ARLINGTON, VA – OCTOBER 16, 2026 – Lidl US is recalling one lot of Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces 16 FL OZ (1 PT) UPC 4 0564897 22458 Lot: 085261 Best By MAR/26/2028 because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women. The recalled product was distributed between 7/19/2026 - 10/15/2026 to all Lidl US retail store locations in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia. The recalled product can be identified as follows: Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces 16 FL OZ (1 PT) UPC 4 0564897 22458 Lot: 085261 Best By MAR/26/2028, which can be found on the bottom of the container. The recalled product is packaged in a clear plastic container with a brown lid. No illnesses have been reported to date. This recall was initiated after routine quality testing identified Listeria monocytogenes present on a lab sample. Customers should immediately discard or return the recalled product to their nearest Lidl store for a full refund (a receipt is not required for return). Customers who have questions about this recall should call the Lidl US Customer Care Hotline at (844) 747-5435, Monday – Saturday between 8 am - 8 pm ET. The health and safety of our customers is our top priority. Lidl US regrets any inconvenience related to this voluntary recall. Our Quality Assurance Department is constantly working to ensure that all products on our shelves meet the high-quality standards that we would expect when feeding our own families. We are grateful for all our Lidl US customers who choose to shop with us every day.

Krasnyi Oktyabr Inc. of Brooklyn, New York, is voluntarily recalling STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED (227g/8oz) packages, because the product has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED (227g/8oz) product was distributed in New York, Florida, Georgia, New Jersey, Pennsylvania and Ohio. The recalled product is identified as follows: Product Name: STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED Brand: STARFISH SEAFOODD Net Weight: 227g/8oz Storage Method: Frozen Packaging: Vacuum-sealed plastic package UPC Code: 4751048940099 Product Code: Best before: 27.11.2027 LOT: D080-148 Country of Origin: Latvia No illnesses have been reported to date in connection with this product. The potential contamination with Listeria monocytogenes was identified by sampling of the product conducted by the New York State Department of Agriculture and Markets. As a result, Krasnyi Oktyabr Inc. initiated a voluntary recall of the affected product. The company is cooperating with the New York State Department of Agriculture and Markets and the FDA regarding the recall. Krasnyi Oktyabr Inc. is a wholesale distributor and did not manufacture the recalled product. The company has notified its affected customers and requested that they immediately discontinue the sale and distribution of the recalled product, identify any remaining inventory, and notify their customers as appropriate. Consumers who have purchased the recalled STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED are urged not to consume the product and to return it to the place of purchase for a full refund. Consumers with questions may contact Krasnyi Oktyabr Inc. at (718) 858-6720, Monday through Friday, from 9:00 a.m. to 5:00 p.m. Eastern Time (ET).

This recall involves the Scotch™ thermal laminator, model number TL1302Z. The laminator is light gray/white with gray accents and the word "Scotch" is printed in gray on the front. The laminating slot is approximately 13 inches wide, and the machine has a carrying handle on the right side of the machine when viewing from the front. The model number TL1302Z is located on the sticker on the bottom of the laminator and can also be found on the product packaging.

This recall involves all units of the Hatsan Blitz and Blitz 777 pellet shooting air rifles sold from February 2020 through March 2026. Both the Blitz and Blitz 777 pellet air rifles were sold in .22, .25 and .30 calibers. The pellet air rifles are gas operated and select-fire (semi-auto/full-auto) pre-charged pneumatic (PCP). They are black and feature a synthetic stock, a carbon fiber air tank mounted beneath the barrel and a rotary magazine feed. Serial numbers and manufacturing dates are engraved on the right side of the receiver above the bolt. On the left side of the receiver is the Hatsan logo, featuring a circular mark, with the word "HATSAN" next to a graphic of a bow and arrow. The model name "BLITZ" or "BLITZ 777" is also marked on the left side of the receiver.

This recall affects Crystal Glass Cups containing loose crystal stone chips between two layers of glass. The cups are intended for both decorative use and drinking. Each cup measures approximately 3.5 by 3 inches. The crystal stone chips are sold in various options: amethyst, black obsidian, rose quartz, smoke quartz, fire and clear quartz, moss agate, hematite, black tourmaline, black tourmaline in quartz, charoite, blue apatite, morganite, larimar, red jasper, malachite, garnet, kunzite, fluorite, peridot, aquamarine, watermelon tourmaline, carnelian, lapis lazuli, tigers eye and labradorite.

This recall involves Papablic bedside sleepers, model PAPA03001AI. These convertible sleepers function as both a bassinet and a play yard and have a gray exterior with an interior printed in a stars‑and‑moon pattern. The products have "Papablic" stitched in white on the front gray fabric panel. Model "PAPA03001AI" is printed on a label sewn to the interior fabric of the bassinet underneath the mattress pad.

This recall involves the Primark 101 Dalmatians Faux Leather Coin Purse, Model No. 2595301. The coin purse is black and has a picture of a dalmatian and "101 Dalmatians" printed on the front. The model number is located on the product tag attached to the zip puller.

This recall involves Xalirium-branded adult portable bed rails. They have a white frame with black foam rubber grips and a black fabric pouch. The bed rails measure about 17.15 inches high, 4.33 inches wide and 1.99 inches long. "Xalirium" is printed on the label of the product packaging. Only bed rails without vertical bars inside the opening are included in this recall.

“This is an update to the company’s press release, previously issued on 10/15/2026, to correct the distribution pattern and serotype of E. coli” WORCESTER, NY, October 15, 2026 - Family Farmstead Dairy of Worcester, NY is recalling specific lot of cheddar cheese because it may be contaminated with Escherichia coli O26:H11 and O45:H2 (E. Coli O26:H11 and O45:H2). E. coli O26:H11 and O45:H2 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death. Product to grocers in NY, PA, NJ, CT, MD, VA, and MA. But the product may also have been distributed to other states via downstream distributors. Affected Product Product: Family Farmstead Dairy Raw Mild Cheddar Cheese Lot Code: 7/22/27 Best By Date: 7/22/27 No other Family Farmstead Dairy products are included in this recall. No illnesses or allergic reactions have been reported to date. The issue was discovered when a LFFM sample in Maryland isolated two strains of Shiga toxin-producing E. coli (STEC) in two samples of Family Farmstead A2 Raw Cheddar, 8 oz package, 7/22/27. Consumer Information Consumers who have purchased the affected product should not consume it. The product should be discarded or returned to the place of purchase for a full refund. At this time, Family Farmstead Dairy has received no reports of illness associated with the recalled product. Consumer Contact Information Consumers with questions regarding this recall may contact: Family Farmstead Dairy Phone: (607) 397-4044 Email: [email protected] 8:30am-5:00pm Easterm, Mon-Fri. "We sincerely apologize to our customers, retail partners, and consumers for the inconvenience caused by this recall. Product quality is an utmost priority here at Family Farmstead so we are committed to identifying the cause of this issue and taking all necessary corrective actions to ensure the continued safety and quality of our products." About Family Farmstead Dairy Family Farmstead Dairy is a New York-based dairy processor dedicated to producing high-quality dairy products while maintaining rigorous food safety and quality standards.

Bayamón, Puerto Rico - Pan Pepín Inc., con sede en Bayamón, Puerto Rico, está retirando voluntariamente del mercado ciertos lotes del producto Para Bien Al Grano debido a que contiene sésamo (ajonjolí), un alérgeno que no fue declarado en su etiqueta. Las personas que tienen alergia o sensibilidad severa al sésamo (ajonjolí) corren el riesgo de experimentar una reacción alérgica grave o potencialmente mortal si consumen este producto. El producto fue distribuido a través de todo Puerto Rico. Información del producto afectado El retiro del mercado incluye los siguientes lotes del producto: PRODUCTO | UPC | #LOT (s) | EXP DATE ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 12 3B1 274 | 10-12-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 14 3B1 277 | 10-14-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 15 3B1 278 | 10-15-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 17 3B1 280 | 10-17-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 18 3B1 281 | 10-18-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 19 3B1 282 | 10-19-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 21 3B1 284 | 10-21-26 Los consumidores con alergia al sésamo (ajonjolí) que hayan adquirido los productos afectados no deben consumirlos. Se recomienda a los consumidores: No consumir los productos si tienen alergia o sensibilidad al sésamo (ajonjolí). Devolver los productos al establecimiento donde fueron adquiridos para recibir un reembolso completo. Desechar los productos si no es posible devolverlos. Comunicarse con la compañía para obtener información adicional sobre el retiro del mercado. Declaración de la Compañía "En Pan Pepín Inc., la seguridad de nuestros consumidores y la transparencia son nuestras principales prioridades. Lamentamos sinceramente cualquier inconveniente que este retiro del mercado pueda ocasionar. Estamos tomando medidas inmediatas para retirar los productos afectados del mercado y reforzar nuestros procedimientos de etiquetado y verificación de alérgenos, con el fin de prevenir incidentes similares en el futuro." Material de Empaque del Producto Vea la imagen a continuación. Enlace a la traducción al inglés

FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 13, 2026 – Par Health is recalling 22 lots of Argatroban Injection 250 mg/2.5 mL (100 mg/mL) to the hospital/user level. This recall is being conducted due to the presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel, that was detected in certain lots. Administration of Argatroban Injection 250 mg/2.5 mL (100 mg/mL) found to contain particulate matter, has a reasonable probability of causing life-threatening adverse health consequences including pulmonary emboli (blockage in pulmonary blood vessels), occlusions of other blood vessels (which can lead to tissue death and possible organ damage), and/or inflammation of the walls of veins, which may lead to clotting. To date, Par Health has not received any reports of adverse events related to this recall. Argatroban Injection 250 mg/2.5 mL (100 mg/mL) is a direct thrombin inhibitor indicated for prophylaxis or treatment of thrombosis in adult patients with heparin-induced thrombocytopenia (HIT) and as an anticoagulant in adult patients with or at risk for HIT undergoing percutaneous coronary intervention. Recalled product can be identified as follows and by representative labels at bottom of this document: Product Description | NDC | Lot | Expiration Date ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 83449 | 10/2026 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 82682 | 11/2026 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 86714 | 02/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 87302 | 02/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 87560 | 02/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 87753 | 03/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 88401 | 03/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 88614 | 04/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 88836 | 04/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 90220 | 05/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 91216 | 06/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 91219 | 06/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 92004 | 07/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 92006 | 07/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 92009 | 08/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 92596 | 08/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 92782 | 08/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 93107 | 08/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 93329 | 08/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-01 | 93890 | 09/2027 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-89 | 84193 | 10/2026 ; Argatroban Injection 250 mg/2.5 mL (100 mg/mL), Distributed by: Par Pharmaceutical* or Endo USA* | 42023-182-89 | 92880 | 08/2027 These lots were distributed nationwide to wholesalers and hospitals between December 30, 2024, and May 5, 2026. Par Health is providing written notification to wholesale and hospital accounts that have received the affected lots and is arranging for return of all existing inventory through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue use and stop distribution. If you have further distributed the recalled product, please notify your accounts or any additional locations which may have received the recalled product. Questions regarding this recall can be directed to Inmar, Inc. at 1-855-648-7909 Monday through Friday between the hours of 9 a.m. and 5 p.m. ET or by email at [email protected]. For medical or technical product information or to report a product complaint or adverse event please call 1-800-828-9393 Monday through Thursday between the hours of 9 a.m. and 8 p.m. ET or Friday between 9 a.m. and 6 p.m. ET. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online: www.fda.gov/medwatch/report.htm Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178 This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Package Identification: See representative examples of vial labels from selected affected lots below: Contacts Gena Holthaus, Senior Director, Corporate Brand and Communications [email protected] *Par Pharmaceutical, Inc. and Endo USA, Inc. are predecessor companies to Par Health USA, LLC, the current distributor of the product.

Pan Pepin Inc. of Bayamón, Puerto Rico is recalling certain lots of Para Bien Al Grano because the product contain sesame. People who have an allergy or severe sensitivity to sesame may risk a serious or life- threatening allergic reaction if they consume these products. The product was distributed throughout Puerto Rico. Affected Product Information The recall involves the following product lots: PRODUCT | UPC | #LOT (s) | EXP DATE ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 12 3B1 274 | 10-12-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 14 3B1 277 | 10-14-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 15 3B1 278 | 10-15-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 17 3B1 280 | 10-17-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 18 3B1 281 | 10-18-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 19 3B1 282 | 10-19-26 ; Para Bien Al Grano | 0 21425 01513 4 | Sell By Oct / 21 3B1 284 | 10-21-26 Consumers with a sesame allergy who have purchased the affected products should not consume them. Consumers are advised to: Not consume the products if they have a sesame allergy or sensitivity. Return the products to the place of purchase for a full refund. Dispose of the products if returning them is not possible. Contact the company for additional information regarding the recall. Company Statement "At Pan Pepin Inc, consumer safety and transparency are our top priorities. We sincerely apologize for any inconvenience this recall may cause. We are taking immediate action to remove affected products from the market and strengthen our labeling and allergen verification procedures to prevent similar incidents in the future." Product Packaging Material See Image Below Consumer Contact Information Consumers with questions regarding this recall may contact: Pan Pepin Inc Telephone: 787-403-7363 Email: [email protected] Hours of Operation: Monday to Friday 8:00am-5:00pm Link to Spanish Translation

Oliva LLC of Bethlehem, CT is recalling approximately 250 units of Riad’s Oliva to Go Baba Ghanouj, Spicy Baba Ghanouj, and Hummus, because it may contain undeclared sesame. People who have an allergy or severe sensitivity to sesame run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled products were distributed to gourmet shops and farm markets in Litchfield County CT and Great Barrington, MA areas. The recalled products are packaged in clear plastic square containers, with a white and green labeling, and best by stamped on side of label. Product Recalled: Riad’s Oliva to Go Baba Ghanouj with best by dates 10/10/26 through 10/14/26 Riad’s Oliva to Go Spicy Baby Ghanouj with best by dates 10/10-26 through 10/14/26 Riad’s Oliva to Go Hummus with best by dates 10/12/26 through 10/18/26 No illnesses have been reported to date in connection with this problem. The recall was initiated after an inspection revealed that sesame was not declared on the product ingredient declaration. Our firm has corrected our labeling since discovering this discrepancy. Consumers who have purchased Riad’s Oliva Baba Ghanouj, Spicy Baba Ghanouj, or Hummus are urged to return it to the place of purchase for a full refund or replacement. Consumers with questions may contact the company at 203-266-5558 8 AM to 4 PM Eastern Monday through Friday.

FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 8, 2026 –Par Health is voluntarily recalling two lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose. Administration of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP), found to contain particulate matter, has a reasonable probability of causing life-threatening adverse health consequences including pulmonary emboli (blockage in pulmonary blood vessels), occlusions of other blood vessels (which can lead to tissue death and possible organ damage), and/or inflammation of the walls of veins, which may lead to clotting. To date, Par Health has not received any reports of adverse events related to this recall. Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) is formulated for intravenous infusion in adult patients or intramuscular induction in pediatric patients. The product is indicated as an ultra-short-acting barbiturate anesthetic primarily used for the induction of anesthesia and procedural sedation. Recalled product can be identified as follows and by labels at bottom of this document: Product | Size | Item Code | Lot Numbers ; Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP), Distributed by: Par Pharmaceutical* | 42023-105-01 | 86930 | 02/2028 ; Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP), Distributed by: Par Pharmaceutical* | 42023-105-01 | 88623 | 04/2028 These lots were distributed nationwide to wholesalers between July 8, 2025 and May 11, 2026. Par Health is providing written notification to wholesale accounts that have received the affected lots and are arranging for return of all existing inventory of Lots 86930 and 88623 through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue use and stop distribution. If you have further distributed the recalled product, please notify your accounts or any additional locations which may have received the recalled product. Questions regarding this recall can be directed to Inmar, Inc. at 1-844-774-1187 Monday through Friday between the hours of 9 a.m. and 5 p.m. ET or by email at [email protected]. For medical or technical product information or to report a product complaint or adverse event please call 1-800-828-9393 Monday through Thursday between the hours of 9 a.m. and 8 p.m. ET or Friday between 9 a.m. and 6 p.m. ET. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online: www.fda.gov/medwatch/report.htm Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178 This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Package Identification: See examples of vial labels from the affected lots below:

This recall involves adult multi-terrain gravel bicycles Van Rysel GRVL AF Sword Brown CN FR (model number 8911304), Van Rysel GRVL AF Apex Beige CN FR (model number 8911305), Van Rysel GRVL AF Sword Pink CN FR (model number 8911308), and Van Rysel GRVL AF GRX Black (model number 8929130). The recalled models were sold in sizes x-small, small, medium, large and x-large. The bicycles are designed for off-road gravel riding, road cycling, commuting and bikepacking. Each bicycle can be identified by the model name and Van Rysel Product ID located on the barcode sticker on the frame near the bottom bracket. Only Van Rysel bicycles with the following Product IDs/ SKUs are included in this recall. Product ID Model Name REI SKU REI Product Name 5476620 USA GRVL AF GRX Black CN FR 2464430001 GRVL AF 2 GRX, GRAPHITE BLACK 5476621 USA GRVL AF GRX Black CN FR 2464430002 GRVL AF 2 GRX, GRAPHITE BLACK 5476622 USA GRVL AF GRX Black CN FR 2464430003 GRVL AF 2 GRX, GRAPHITE BLACK 5476623 USA GRVL AF GRX Black CN FR 2464430004 5476624 USA GRVL AF GRX Black CN FR 2464430005 GRVL AF 2 GRX, GRAPHITE BLACK 5327224 USA GRVL AF Apex Beige CN FR 2464440001 GRVL AF 2 Apex, CREAM BEIGE 5327225 USA GRVL AF Apex Beige CN FR 2464440002 GRVL AF 2 Apex, CREAM BEIGE 5327226 USA GRVL AF Apex Beige CN FR 2464440003 GRVL AF 2 Apex, CREAM BEIGE 5327227 USA GRVL AF Apex Beige CN FR 2464440004 GRVL AF 2 Apex, CREAM BEIGE 5327228 USA GRVL AF Apex Beige CN FR 2464440005 GRVL AF 2 Apex, CREAM BEIGE 5327239 USA GRVL AF Sword Pink CN FR 2464450001 GRVL AF 2 Sword, GRANITE PINK 5327240 USA GRVL AF Sword Pink CN FR 2464450002 GRVL AF 2 Sword, GRANITE PINK 5327241 USA GRVL AF Sword Pink CN FR 2464450003 GRVL AF 2 Sword, GRANITE PINK 5327242 USA GRVL AF Sword Pink CN FR 2464450004 GRVL AF 2 Sword, GRANITE PINK 5327243 USA GRVL AF Sword Pink CN FR 2464450005 GRVL AF 2 Sword, GRANITE PINK 5327219 USA GRVL AF Sword Brown CN FR 2464450006 GRVL AF 2 Sword, CORIANDER BROWN 5327220 USA GRVL AF Sword Brown CN FR 2464450007 GRVL AF 2 Sword, CORIANDER BROWN 5327221 USA GRVL AF Sword Brown CN FR 2464450008 GRVL AF 2 Sword, CORIANDER BROWN 5327222 USA GRVL AF Sword Brown CN FR 2464450009 GRVL AF 2 Sword, CORIANDER BROWN 5327223 USA GRVL AF Sword Brown CN FR 2464450010 GRVL AF 2 Sword, CORIANDER BROWN

This recall involves DR Power Equipment Pilot and Premier walk-behind trimmer mowers. The trimmer mowers are orange and black and have the DR Power logo on the top of the motor and on the top of the frame above the cutter head. The trimmer mowers are labeled "Premier" or "Pro" on the side of the frame. The model numbers are printed on a label located on the side of the product's frame. Recalled model numbers and product description, which include all serial numbers, are listed below. Model Number Product Description Serial Number Range T4X1076DMN DR TRIMMER PILOT 7.6 FPT DR MS All T4X1076DMNR DR TRIMMER PILOT 7.6 FPT DR MS RECON All T4X1076DMNSD DR TRIMMER PILOT 7.6 FPT DR MS SD All T4X1176DMN DR TRIMMER PILOT 7.6 FPT DR MS All T4X1176DMN-1 DR TRIMMER PILOT 7.6 FPT DR MS All T4X1176DMNR DR TRIMMER PILOT 7.6 FPT DR MS RECON All TR43076DMN DR TRIMMER PREMIER 7.6 FPT DR MS All TR43076DMNR DR TRIMMER PREMIER 7.6 FPT DR MS RECON All

October 8, 2026, Gardeners Basics of Spanish Fork, Utah, is recalling one-pound bags of broccoli sprouting seeds because they may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. The product was distributed nationwide in the United States through online sales and shipped directly to consumers. The product was sold online through Amazon, www.gardenersbasics.com, TikTok Shop, Walmart, eBay and Etsy. Sales have stopped. Consumers should identify recalled bags using the product name, package and marking described below. The recalled product is Gardeners Basics Waltham 29 Broccoli Sprouting Seeds, packaged in a white and green resealable pouch, net weight 1 pound (454 g), with UPC 848137042889. The bag is marked "Packed for 2027." On September 26, 2026, Gardeners Basics was notified by our seed supplier that bulk broccoli seed lot #W4105 was recalled because Salmonella was detected in a broccoli seed sample that was collected and analyzed by the FDA. Additionally, the seeds were identified as being used by a sprout grower whose finished product was part of an FDA investigation involving a multistate foodborne illness outbreak. No illnesses related to this product had been reported to Gardeners Basics as of October 6, 2026. Sales of the affected product have stopped. Consumers should stop using the recalled seeds and they should not eat the seeds or any sprouts grown from them. Consumers should: Seal the recalled seeds and any sprouts in a bag and discard them. No return is required. Contact Gardeners Basics for recall assistance or a refund if your affected purchase has not already been refunded. If you are unsure whether your bag is affected, stop using it and contact us. Please provide your order number and where you purchased the product. Email [email protected], or text or leave a voicemail at 801-769-6181 any time, seven days a week. Live calls are not answered. FDA Advisory