989 recalls tagged with “adult product”.
Amy's Kitchen recalled 38,856 frozen Gluten Free Bean & Rice Burritos across 3,238 cases distributed to 21 states on Oct. 2, 2025. The recall cites potential contamination with foreign objects. Consumers should not eat the product and should contact Amy's Kitchen for refund or replacement information.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.
Church & Dwight recalled 21,912 bottles of ZICAM Cold Remedy Medicated Fruit Drops Elderberry from nationwide distribution in the United States. The label did not indicate elderberry as an ingredient though the product contains elderberry. Consumers should stop using the product and contact Church & Dwight for guidance.
Ocean's Kitchen recalled 496 cases of imitation crab meat shredded, distributed in Washington state. The product is refrigerated and vacuum-packaged. The recall cites potential contamination with Clostridium botulinum due to temperature abuse during chilled storage. Consumers should not consume the product and should contact Oceans Kitchen for refunds or replacements.
AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.
Dr. Reddy's Laboratories Inc. recalled 571 vials of Succinylcholine Chloride Injection, USP nationwide in the United States. The recall cites an out-of-specification result during six-month stability testing due to decreased preservative concentration. Healthcare providers and patients should stop using the product immediately and await guidance from the recall letter.
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.
Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.
Reser’s Fine Foods recalled 3,252 cases of Basil Pesto Bowtie Pasta Kit Item V, UPC 13454 38053, distributed in AZ, CA, CO and TX. The recall concerns potential contamination with Listeria monocytogenes. Consumers should not eat the product and should seek refund or replacement.
Wholesale Produce Supply LLC DBA recalled 307 cases of Cut Fresh Melon Mix due to potential Listeria monocytogenes contamination. The recall covers multiple Melon Mix products packed by WPS in Minneapolis and distributed to IA, IL, ND, NE, and WI. Consumers should not eat the product and should seek refunds or replacements.
Albertsons Companies recalled store-made Basil Pesto Bow Tie Pasta Salad sold under banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons after Listeria monocytogenes contamination. The bowtie pasta ingredient used in the deli item was recalled for this reason. Consumers who purchased the product should not consume it and should contact Albertsons Companies for refund or
Albertsons recalled store-made Ready Meals Pesto Bowtie Pasta Salad sold at banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb and Vons. The recall concerns a bowtie pasta ingredient contaminated with Listeria monocytogenes. Do not consume the product and seek a refund or replacement from Albertsons Companies LLC.
A high-risk recall affects 795 cases of Reser’s Fine Foods Basil Pesto Bowtie Pasta Kit distributed in Arizona, California, Colorado, Utah and Washington. The recall covers item #404736 with use-by dates in October 2025. Consumers should not consume these salad kits and should contact Reser’s for refunds or replacements.
Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad sold under Carrs-Safeway, Eagle and Safeway banners in Alaska and 14 other states after the FDA linked the product to Listeria monocytogenes. The in-store Penne pasta ingredient recall prompted the action. Consumers should not eat the product and should contact Albertsons Companies LLC for refund or replacement.
Wholesale Produce Supply LLC DBA recalled 307 cases of Cut Fresh Fruit with Fruit Dip sold under Fresh & Finest and Harvest Cuts. The fruit was distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The recall follows a potential Listeria monocytogenes contamination. Consumers should not eat the product and should contact Wholesale Produce Supply LLC DBA for refunds or replacements.