2,153 recalls tagged with “stop use immediately”.
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.
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.
Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.
Astemrey recalls Y'all Can DIY bioethanol fireplace liquid fuel containers sold through unknown retailers due to a deadly flash-fire risk. The containers lack flame-mitigation devices required by safety standards. Stop using the product immediately and contact Astemrey for a free replacement.
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.
Diasol recalled 2,200 gallons of its 100425-10-DEX100 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.
Diasol recalled 7,200 gallons of its 100125-10-DEX100 liquid concentrate on November 5, 2025. The recall affects dialysis patients in multiple states due to unassured safety and efficacy. Patients and healthcare providers must stop using this product immediately.
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.
The Maros Group is recalling 24 bottles of Prickly Pear Jelly sold in Arizona. The recall stems from undeclared milk in the product. Consumers should not eat it and should contact The Maros Group for a refund or replacement by telephone.
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.
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.
Mama Rose's Prickly Pear Salad Dressing, distributed by The Maros Group, LLC in Arizona, is recalled. The issue is undeclared sulfites in the dressing. Consumers should stop using it and contact The Maros Group for refund or replacement.
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.
Ford recalled certain 2025 Explorer SUVs due to a powertrain control module software fault. The PCM may reset while driving, potentially damaging the park system or causing an engine stall. Dealers will perform a free software update after owner letters were mailed on June 6, 2025.
Africa Imports recalled 31 units of Organic Moringa Leaf Powder after Salmonella was detected in one lot. The recall covers 4 oz containers and 1 kg bags distributed to 14 states and the District of Columbia. Consumers should stop using the product and contact Africa Imports for refunds or replacements.
Hyundai Motor America recalls 2025 Hyundai IONIQ 5 N vehicles with left-foot braking and N e-shift features. The recall cites potential reduced braking performance and continued acceleration after pedal release. Owners should avoid LFB and N e-shift until remedy is complete. OTA or dealer updates are free.
Datascope recalled 11,470 Intra-Aortic Balloon Pump systems on November 4, 2025. The recall addresses a revision in the Preventative Maintenance schedule as outlined in the Service Manual. Healthcare providers and patients must stop using these devices immediately.
GET TESTED INTERNATIONAL AB recalled 31 Leaky Gut Test devices distributed nationwide in the United States after the product was found to be distributed without FDA premarket approval. The devices test for gut health but lack FDA clearance. Consumers should stop using the device immediately and contact the manufacturer for instructions.
GET TESTED INTERNATIONAL AB recalled 754 units of a 2 in 1 Trichomonas / Gardnerella Test distributed nationwide in the United States after regulators found distribution without premarket approval or clearance. The device was distributed without FDA clearance. Patients and healthcare providers should stop using the test immediately and follow the manufacturer’s recall instructions by contactingGET