2,056 recalls tagged with “cpsc regulated”.
In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.
Leprino Foods recalled 5,453,442 pounds of LMPS bulk mozzarella distributed to Ohio, Tennessee, Texas, Utah and Wisconsin after the FDA enforcement notice. The recall cites the possible presence of stainless steel pieces in the product. Consumers should not consume the mozzarella and should contact Leprino Foods for refund or replacement information.
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
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.
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.
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.
SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.
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.
B BRAUN MEDICAL recalled 1,298,454 STREAMLINE BLOODLINE SET FOR DIALOG devices nationwide in the United States after observations of micro-air bubbles and air-in-line alarms linked to damaged arterial and venous connectors. The defect increases the risk of air entering the bloodstream during dialysis. Patients and healthcare providers should stop using this device immediately and follow the recall
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.
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.
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.
Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.
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.
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.
Albertsons recalled store-made Spinach Bowtie Pasta Salad due to Listeria monocytogenes. The recall covers deli items made in-store with scale-labels across banners including Albertsons, Amigos, Market Street, United in NY and TX. Consumers should not eat the product and should contact Albertsons for refund or replacement.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix sold through multiple retailers in Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The recall covers two brand variations and multiple lot numbers with October 2025 expirations. Consumers should not consume the product and should contact Wholesale Produce Supply LLC DBA for refund or replacement information.
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.