794 recalls tagged with “infant product”.
Tegu recalled two Magnetic Floating Stackers sold at multiple retailers. Models STA-BGY-801T and STA-BTP-806T are affected. The magnets can detach and be ingested, posing a serious injury or death risk. Parents should stop using the toys immediately and contact Tegu for a free replacement.
Backyard Kids recalled KidKraft Farm to Table Play Kitchens in 2025 after one death was reported at multiple retailers. The hazard arises from hooks that hold toy accessories where clothing can snag during climbing or crawling through the back opening. Stop using the play kitchen immediately and contact Backyard Kids for free replacement hooks or repair.
Eight modular LinkSymphoKnee TiNbN tibial components are under recall after production with two uncoated security screws. Waldemar Link GmbH & Co. KG disclosed the issue. The devices were distributed worldwide, including CO, IN, NJ and TX in the United States, plus Germany and Italy. Consumers should stop using the device immediately and follow manufacturer instructions.
Medline Industries recalled 7,913 reprocessed Inquiry Steerable Diagnostics Catheters due to contamination risks. Some models may contain small residual particulates that can cause severe inflammatory responses or systemic infections. Patients must stop using these devices immediately and contact healthcare providers for further instructions.
Medline Industries recalled 7,913 reprocessed Webster CS Catheters for electrophysiology mapping nationwide in the United States. The recall concerns small residual particulates on patient-contacting surfaces that could trigger inflammatory responses or systemic infection. If particulates dislodge and contact circulating blood or the heart, they could cause granulomatous reactions or thrombus, and
Medline Industries recalled 7,913 reprocessed ACUSON AcuNav ultrasound catheters nationwide in the United States. The recall cites residual particulates on patient-contacting surfaces as the hazard. Consumers should stop use and follow manufacturer instructions for recall actions.
Fortress Introducer Sheath System recalled 2,500 units linked to label mispackaging. The devices were distributed worldwide, including 15 U.S. states and numerous international markets. The incorrect pouch label lists the 4F version reference and unique device identifier instead of the packaged 6F version. Healthcare providers must stop use and follow manufacturer recall instructions.
Exela Pharma Sciences recalls 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10 mL, nationwide in the U.S. The recall cites out-of-spec arsenic impurities. Consumers should stop use and contact a healthcare provider. Follow recall notice for guidance and refunds.
Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.
VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病
Dynamic Sports Nutrition recalled 1,566 bottles of WINN-50 vanazolol dietary supplement sold nationwide. The FDA-listed recall cites degradation of an ingredient and sub-potent Vitamin B12. Consumers should stop using the product and contact the company for refunds or replacements.
Medline Industries, LP recalled 2,520 Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles sold to U.S. hospitals and healthcare facilities. The lights on the handles may fail to illuminate as intended. Hospitals should stop using the devices immediately and follow recall instructions.
Zap Surgical Systems recalled 17 ZAP-X Radiosurgery System units worldwide, including US states FL, CO, NJ, NY and several countries. A software defect could cause the collimator to collide with patient shoulders or the patient table during long gantry moves after proximity errors. Clinicians and patients should stop using the device and follow recall instructions from the manufacturer.
Pura Scents recalled the Pura 4 Smart Home Fragrance Diffusers sold at retailers on July 24, 2025. The detachable cover contains five magnets and can detach, creating an ingestion hazard for children. Consumers should stop using the diffuser immediately and contact Pura Scents for a free replacement front cover.
Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets sold at retailers due to a button cell battery ingestion hazard. The recall covers models 718508MCR and 718075MCR. Consumers should stop using the recalled bracelets immediately and email disposal photos to info@innovativenyc.com to receive a full refund.
Transpro US recalls three scooter models sold with unauthorized lithium-ion battery UL certification labels. The recall covers A3 Hub Motor, A11F Spark, and R1 Commuter scooters. Consumers should stop using these scooters immediately and contact Transpro for a refund or replacement.
Diamond G Forest Products recalled 4-ounce turpentine bottles. The Georgia Pine Gum Spirits of Turpentine label appears on the recalled bottles. The packaging is not child-resistant, violating federal law. Consumers should stop using the product and contact the company for a free closure replacement.
Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.
LIVACTI LT-BG01-3 retractable safety gates sold on Amazon by Qeyan and Yanyanny are recalled for entrapment risk. The recall notes the gate violates the mandatory safety standard for gates and enclosures. Stop using the gate immediately and contact the sellers for a full refund.
Minongad recalled LED Gloves model ST01 after safety violations exposed battery ingestion risk. The recall covers gloves sold on Amazon with two pre-installed lithium coin batteries and four spare batteries. Consumers should stop using the gloves immediately and return them for a full refund.