495 recalls tagged with “suffocation risk”.
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Toyota recalls 2022-2025 Tundra and Tundra Hybrid vehicles because moisture in the reverse light assemblies can cause light failure. Dealers will replace both reverse light assemblies and repair wire harnesses. Owner letters were mailed September 11, 2025. Contact Toyota at 1-800-331-4331 for recall 24TB06 and 24TA06.
Philips Respironics recalls 113,717 Trilogy Evo O2 home-use ventilators in 2026. The Obstruction Alarm may fail to trigger within required standards, delaying warning for airway obstruction for up to four breaths. Stop using the device and follow recall instructions from Philips or your clinician.
Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.
Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.
Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.
Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.
Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek
Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.
Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.
Medline Industries, LP recalls 108 NAMIC Angiographic Rotating Adaptor Syringes sold worldwide, including the United States, PR and several international markets. The rotating adaptor may unwind during use, creating a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions.
Medline Industries, LP recalled 594 medical convenience kits worldwide, including NAMIC Angiographic Rotating Adaptor syringes, due to a potential unwinding of the syringe adaptor that can cause a loose connection or disconnection with the manifold.
Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed
Medline Industries recalled 2,630,369 NAMIC Angiographic Syringes worldwide after post-market surveillance found a potential risk that the syringe rotating adaptor could unwind during use, causing a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions. Contact Medline or a healthcare provider for guidance.
Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan
Medline Industries, LP recalls 966 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers kits labeled DELIVERY PACK with SKUs DYNJ42892F and DYNJ42892G distributed worldwide, including the US and PR. The defect is a rotating adaptor that may unwind, creating a loose connection or disconnection between syringe and manifold. Stop using the device and use
Kaiwenshangpin recalled magnetic chess games on February 26, 2026, due to a serious ingestion hazard. The games contain loose magnets that can pose a risk of injury or death to children. Consumers should stop using the product immediately and return it for a full refund.
Zelbuck recalled children's chess games on February 26, 2026, due to a serious ingestion hazard. The games contain loose magnets that can lead to serious injury or death if swallowed. Consumers should stop using the games immediately and seek a full refund.
Sanven Technology recalled Vevor-branded safety gates on February 26, 2026. The gates pose an entrapment hazard that could lead to serious injury. Consumers should stop using the gates immediately and contact the company for a full refund.
Bicystar recalled children's high chairs on February 26, 2026, due to serious fall and entrapment hazards. The affected high chairs lack required crotch restraints, putting children at risk. Consumers should stop using these chairs immediately and seek a refund.