1,215 recalls tagged with “replacement available”.
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.
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.
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.
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.
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.
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.
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.
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.
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.
GET TESTED INTERNATIONAL recalled 3 Gut Microbiome Test Large kits sold nationwide in the United States after regulators flagged distribution without premarket approval. The recall centers on a lack of FDA clearance for the device. Consumers and healthcare providers should stop using the device immediately and follow recall instructions.
GET TESTED INTERNATIONAL AB recalled 3 Food Sensitivity Test Small units distributed nationwide in the United States after a lack of premarket approval was identified. The recall is classified as Class II with a high-level hazard. Consumers should stop using the product immediately and follow the recall instructions from the manufacturer.
Fresenius Kabi USA recalls 483 LVP Primary Infusion Sets for the IVENIX infusion system nationwide in the United States. The recall cites incorrect assembly of a specific lot. Hospitals and clinicians should stop using the affected sets immediately and follow the manufacturer’s recall instructions.
Nissan North America, Inc. recalls certain 2025 Sentra vehicles. The driver’s seat frame may not be fully secured to the outer side of the seat track, potentially failing to meet FMVSS 207 and 210. Dealers will inspect and replace the driver's side lower seat frame assembly as necessary at no charge; owner letters were mailed May 1, 2025.
GET TESTED INTERNATIONAL AB recalled 16 Food Intolerance Test Medium devices distributed nationwide in the United States. The devices were distributed without premarket approval or clearance. Consumers should stop using the device immediately and follow the manufacturer’s recall instructions.
GET TESTED INTERNATIONAL AB recalled 1,916 Thyroid TSH Tests distributed nationwide in the United States. The devices were distributed without premarket approval or clearance. Healthcare providers and patients should stop using the tests and follow manufacturer instructions immediately.
GET TESTED INTERNATIONAL AB recalled a single Sperm Test device distributed nationwide in the United States on 2025-11-03 due to distribution without FDA premarket approval or clearance. The device was not cleared for sale in the U.S. The company classified the recall as active. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall guidance
100% of reported issues involve distribution without premarket approval. GET TESTED INTERNATIONAL AB’s HbA1c Diabetes Test was distributed nationwide in the United States without FDA clearance. Stop using the product immediately and follow the manufacturer’s recall instructions.
Get Tested International AB recalled 1,210 units of its 3 in 1 STI Test distributed nationwide in the U.S. The product was distributed without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.,
GET TESTED INTERNATIONAL AB recalled 166 units of its Candida Test distributed nationwide in the United States. The device was distributed without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the recall instructions from the manufacturer.
GET TESTED INTERNATIONAL AB recalled 3 units of its Food Allergy Panel Test (IgE) distributed nationwide in the United States after distribution without premarket approval was identified. The recall pertains to a regulatory lapse rather than an announced safety defect. Consumers should stop using the device immediately and follow manufacturer instructions.