794 recalls tagged with “infant product”.
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.
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.
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.
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.
Laiwu Manhing Vegetables Fruits Co recalled 245 cartons of irradiated onion granules sold in California after foreign objects were found in the powder. The contamination is described as black plastic planting film. Consumers should not consume the product and should contact the company for refund or replacement via email.
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.
GET TESTED INTERNATIONAL AB recalled 658 parasite tests distributed nationwide in the United States after regulators flagged distribution without premarket approval. The recall, active as of December 2025, targets devices labeled EAN 7340221707153 and SKU A-PARA. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.
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.
GET TESTED INTERNATIONAL AB distributed 1 unit nationwide in the United States. The device lacked premarket approval or clearance. Stop using the product immediately and contact GET TESTED INTERNATIONAL AB for 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 6 Food Intolerance Test Large units sold nationwide in the US after a premarket approval issue. The device was distributed without premarket approval or clearance. Consumers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB or their healthcare provider for instructions.
GET TESTED INTERNATIONAL AB recalled 1,218 D-Dimer Test kits nationwide after distributing without premarket approval. The recall cites distribution without FDA premarket approval or clearance. Healthcare providers and patients should stop using the device immediately and follow all recall instructions.
GET TESTED INTERNATIONAL AB recalled 2 Gut Microbiome Test Mega units distributed nationwide in the United States. The recall centers on distribution without premarket approval or clearance. Consumers should stop using the device and contact the manufacturer for instructions. The notice was issued in 2025 and is currently active.
GET TESTED INTERNATIONAL AB's gonorrhea test was distributed nationwide in the United States. The recall cites distribution without FDA premarket approval or clearance. Patients and healthcare providers should stop using the test immediately and follow the manufacturer's recall instructions.
GET TESTED INTERNATIONAL AB recalled 36 NAD Profile Tests distributed nationwide in the United States after regulators found distribution without premarket approval. The devices were distributed without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow recall instructions; contact GET TESTED INTERNATIONAL AB or your health‑ca
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
GET TESTED INTERNATIONAL AB recalled 115 ferritin iron deficiency tests distributed nationwide in the United States. The tests were distributed without FDA premarket approval or clearance. Stop using the device immediately and contact GET TESTED INTERNATIONAL AB or your healthcare provider for instructions.