2,756 recalls tagged with “immediate action”.
Ventura Foods recalls 3,556 cases after discovering foreign objects in granulated onion. Distribution covered 42 U.S. locations and Costa Rica. Consumers should not eat the product and should seek refund or replacement from Ventura Foods.
Peloton recalled Original Series Bike+ units with model PL02 and serials beginning with the letter 'T'. The seat post assembly can break during use, creating a fall and injury risk. Consumers should stop using the recalled bikes and contact Peloton for a free repair.
Inkari recalled plush alpaca toys sold through multiple retailers after eyes detach, creating a choking hazard for children under three. The eyes can detach, violating the small parts ban. Consumers should stop using the recalled plush toys and contact Inkari for a full refund.
Criblike recalled three infant mattresses sold on Amazon by Mengna for entrapment and suffocation risk. The Pack and Play mattresses are XCD-001 and XCD-002. The Mini-Crib mattress is MNCL-001. The products measure 38 by 26 inches and 38 by 24 inches, respectively. Stop using them and contact Criblike for a full refund.
C.R. Bard Inc recalled 116 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall stems from a labeling discrepancy where the actual stent size may not match the product label. This recall affects distribution in multiple U.S. states and several countries worldwide.
Sanven Technology recalls 3 Vevor Baby Swing models on 2025-11-06 for a suffocation risk linked to an incline greater than 10 degrees. The swings carry the VEVOR trademark and are labeled as Multi-Function Electric Swing with model numbers BB501K, BB702A, and BB005. Consumers should stop using the swings immediately and contact Sanven Technology for a full refund.
STIHL is recalling BR 800 Magnum backpack blowers sold through authorized STIHL dealers from May 2025 through September 2025. The recall targets units with serial numbers 546515117 to 547916107. The fan wheel inside the blower can break apart, creating a laceration hazard. Consumers should stop using the recalled units and bring them to an authorized STIHL servicing dealer for a free inspection is
F&F Fine Wines is recalling Kirkland Signature Valdobbiadene Prosecco DOCG bottles sold at Costco due to a laceration hazard from potential breakage. The recall covers UPC 196633883742 and Costco Item Number 1879870. Consumers should stop using recalled bottles immediately and contact Ethica Wines for refund instructions from Costco.
Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.
Lezyne USA recalls two bicycle floor pumps, the Pressure Over Drive and Digital Pressure Over Drive, sold at bicycle stores nationwide and online. The canister can eject from the base when pressurized, posing a serious injury risk. Stop using the recalled pumps and contact Lezyne for a free replacement.
CareFusion 303 recalled 189 BD Alaris Pump Modules on November 6, 2025. The recall affects connectivity to hospital networks due to daylight savings time adjustments. Users should stop using the device immediately and follow manufacturer instructions.
C.R. Bard recalled 4,350 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall was initiated due to a labeling discrepancy where the actual size of the stent may not match its label. This affects distribution across the U.S. and several countries worldwide.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual size of the stent to differ from what is indicated on the label. The recall affects distribution across the U.S. and several countries worldwide.
Bard Peripheral Vascular recalled 1,240 Safe-T-Centesis Catheter Drainage Trays due to safety indicator defects. The recall affects products distributed nationwide since November 6, 2025. The defect may cause serious injuries during use in medical procedures.
Diasol recalled 4,400 gallons of its 100230-10-DEX100 dialysis acid concentrate on November 5, 2025. The company cannot assure the safety and efficacy of this product. Healthcare providers and patients must stop using the concentrate immediately.
Lupin Pharmaceuticals recalled 52,128 bottles of Sertraline Hydrochloride Tablets on November 5, 2025. Consumers reported issues with defective seals that do not adhere to the bottles. The recall follows a Class II classification due to potential contamination risks.
Diasol recalled 186,000 containers of its liquid concentrate for bicarbonate dialysis on November 5, 2025. The company cannot assure the safety and efficacy of the product. Patients and healthcare providers should stop using it immediately and follow recall instructions.
Diasol recalled 4,400 gallons of its dialysis liquid concentrate on November 5, 2025. The recall follows concerns that the safety and efficacy of the product cannot be assured. Healthcare providers and patients should stop using the product immediately.
Diasol recalled 74,400 gallons of its Liquid Concentrate for Bicarbonate Dialysis on November 5, 2025. The recall stems from concerns about the safety and efficacy of the dialysis acid concentrate. Patients and healthcare providers should stop using the product immediately.
African Food on Wheels Inc. recalled 20 boxes of Oven Dried Fish on November 5, 2025. The product poses a high risk of Clostridium botulinum contamination. Customers should not consume the fish and seek a refund immediately.