495 recalls tagged with “suffocation risk”.
B. Braun Medical Inc. recalls 74,088 Lactated Ringers Injection USP containers nationwide over sterility concerns. The recall cites potential fluid leakage at weld sites and lack of assurance of sterility. Healthcare providers and patients should stop use and seek guidance from their supplier or provider immediately.
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.
Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.
Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.
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
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.
S.I.N. Implant System Ltda recalled 4,367 dental implants after reports of potential packaging damage. Improper temperature and storage conditions may compromise product quality and performance. Patients and healthcare providers should stop using these implants immediately and follow the manufacturer's instructions for return.
BMW recalls 2025 motorcycles with optional eCall system due to a software error that can deactivate emergency crash notification. OTA or dealer update will fix the issue. Letters to owners go out Sept. 12, 2025. Contact BMW at 1-800-525-7417.
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.
Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.
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.
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.
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.
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.
Creekwood Naturals recalled Gum Spirits of Turpentine bottles, with no retailer named in the notice. These bottles violate the Poison Prevention Packaging Act by lacking a child-resistant closure. Consumers should stop using the product and request a free replacement closure from Creekwood Naturals.
BMW of North America recalls 2022–2025 i4, 2022–2024 iX, 2023–2024 i7, and 2024 i5 vehicles over software that may shut down the high-voltage system, causing loss of drive power. OTA software updates or dealer service will fix the issue at no cost. Letters to owners begin August 5, 2025.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.