1,215 recalls tagged with “replacement available”.
Coca-Cola Southwest Beverages LLC recalls 1,115 units of Coca-Cola Zero Sugar 12oz cans sold in Texas. The cans may contain metal fragments. Consumers should not drink the product and should contact the company for refund or replacement.
Food Club recalled 117 cases of Finely Shredded Pizza Style Four Cheese Blend, sold at multiple retailers nationwide, after potential metal fragments were found in a supplier raw material. The 8-ounce packages contain mozzarella, provolone, parmesan and romano cheeses and carry UPC 3680017231. Consumers should not eat this product and should contact Great Lakes Cheese Co for refund or replacement.
Blossom recalled two-piece children’s loungewear sets sold under its brand due to a burn risk that violates the mandatory flammability standard for children's sleepwear. The recall covers sets in multiple colors and designs sold for sizes 12 months through 12 years. Stop using the garments and contact Blossom for a full refund.
Zyntony recalled Kogalla power banks sold on Kogalla.com due to fire and burn hazards. The recall targets BP125, BatPak 2F and BatPak 3F models. The lithium-ion batteries can overheat and ignite, even when not in use. Consumers should stop using the recalled power banks and contact Kogalla for a free replacement.
Gunaito recalled 10-drawer dressers sold on Walmart.com after reports of tip-over and entrapment hazards. The recall targets brown and white dressers with model numbers HD006BN-SLCD and HD006WH-SLCD. The product packaging bears the codes HD006BN-SLCD or HD006WH-SLCD.
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.
DEMERS FOOD GROUP LLC is recalling Scott & Jon's Shrimp Scampi with Linguine, 9.6 oz, sold nationwide. The linguine component, manufactured by Nate's Fine Foods LLC, was recalled for Listeria monocytogenes and linked to an ongoing outbreak. Consumers should not consume the product and should contact DEMERS FOOD GROUP LLC for refund or replacement using email, fax, letter, press release, telephone,
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.
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.
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
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.
Acella Pharmaceuticals recalls doxycycline hyclate tablets, 100 mg, 500-count bottles distributed nationwide in the USA. Stability testing found the lot did not meet dissolution specifications. Consumers and healthcare providers should stop using the product immediately and contact Acella 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.
Wholesale Produce Supply LLC recalls Fresh & Finest Luau Blend Fruit Mix after potential Listeria monocytogenes contamination. The recall covers 307 pails distributed to retailers in Iowa, Illinois, North Dakota, Nebraska and Wisconsin. Consumers should not eat this product and should contact Wholesale Produce Supply LLC DBA for refunds or replacements.
The Kroger Co is recalling 25,792 pounds of Smoked Mozzarella Penne Salad sold at Kroger banners nationwide after FDA notices potential Listeria monocytogenes. Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact The Kroger Co for refund or replacement information by
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.
Kroger recalled 5,567.4 pounds of Basil Pesto Bow Tie Pasta Salad sold at Kroger banners across 28 states after potential Listeria monocytogenes contamination. The pasta ingredient used in these deli items was recalled due to the contamination risk. Consumers should not eat these products and should contact The Kroger Co for refund or replacement via email.
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.