495 recalls tagged with “suffocation risk”.
Covidien recalled 78 HealthCast Vital Sync Remote Patient Monitoring Systems sold worldwide, including in the United States. Alarms from the bedside monitor may not alarm or transmit to the remote system. Healthcare providers and patients should stop using the device immediately and await recall instructions.
BD recalled 204,000 10 mL Luer-Lok/Luer Slip syringes due to a packaging mix-up that placed Luer Slip syringes in a batch designated for Luer Lok syringes. The nationwide recall covers products distributed in California and Texas. Healthcare providers and patients should stop using the affected syringes immediately and consult manufacturer recall instructions.
ITS GmbH recalled 510 units of the I.T.S Straight Plate with Angular Stability after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The recall covers multiple article numbers across forearm and straight plates and distributions nationwide in the United States. No injuries or incidents have been reported at this time. Healthcare providers andpatients
ITS recalls 70 Olecranon Plates with Angular Stability distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using this device immediately and contact ITS or their healthcare provider for instructions.
I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.
ITS GmbH recalls 101 Pilon Plate with Angular Stability implants distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
ITS GmbH recalled 176 units nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The issue could cause burns during MRI exposure. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Based Online recalled Fidget Magnet Ball Toy Sets on January 22, 2026, due to a serious ingestion hazard. The toys contain loose high-powered magnets that pose risks of severe injury or death if swallowed. Consumers should stop using these toys immediately and seek a refund.
Mikario Trading recalled 5,000 convertible baby gyms on January 22, 2026, due to a suffocation risk. The baby gyms violate safety standards for infant support cushions. Consumers must stop using the product immediately and seek a refund.
Aborder Products recalled Cumbor retractable safety gates on January 22, 2026, due to a serious entrapment risk for children. The gates can allow a child's torso to fit through the opening, posing a high risk of injury or death. Consumers must stop using the gates immediately and contact the company for a full refund.
Gagaku recalled ice cream shop toy playsets on January 22, 2026, due to a magnet ingestion hazard. The toys can pose serious injury or death risks if magnets detach and are swallowed. Consumers should stop using the toys and seek a refund immediately.
Instrumentation Laboratory recalls 8 GEM Premier 5000 cartridges worldwide after PCSND warm-up errors cause GEM PAK ejections. The defect may prolong turnaround times and delay results. Hospitals and clinics should stop using the device and contact the manufacturer for instructions.
Instrumentation Laboratory recalls 489 GEM Premier 5000 PAK cartridges worldwide after reports of Process Control Solution Not Detected errors during warm-up. iQM2 monitors the testing process and may allow continued use after AutoPAK Validation. The recall highlights potential operational disruptions in patient management.
Instrumentation Laboratory issued a high-severity recall for 1,126 GEM PAK cartridges used with the GEM Premier 5000. The recall cites increased PCSND errors during warm-up that can cause consecutive GEM PAK ejections. The issue may delay patient results. Hospitals should halt use and follow manufacturer instructions immediately.
Instrumentation Laboratory recalled 51 GEM Premier 5000 PAK cartridges worldwide after complaints of PCSND errors during warm-up. These errors can cause GEM PAK cartridges to eject. The recall could delay results and affect patient management. Stop using the affected cartridges and follow recall instructions from Instrumentation Laboratory.
A worldwide distribution recall covers 74 GEM PAK cartridges for the GEM Premier 5000. The issue involves PCSND errors during warm-up that can trigger ejection of GEM PAKs and may delay results. Institutions should follow recall instructions from Instrumentation Laboratory and notify healthcare teams immediately.
BBWOO recalled baby loungers on January 15, 2026, due to serious injury risks. The loungers violated safety standards, posing entrapment and fall hazards. Consumers should stop using the product immediately and seek a refund.
Greatale recalled self-feeding pillows on January 15, 2026, due to a serious risk of aspiration and suffocation in infants. The pillows can hold a bottle at an unsafe angle, preventing infants from pulling away. Consumers must stop using the pillows immediately and return them for a full refund.
Yixing Trading recalled KEAWIS crib mattresses on January 15, 2026. The mattresses pose a suffocation and entrapment hazard due to improper fit in cribs. Consumers should stop using the mattresses immediately and seek a refund.
R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.