suffocation risk Recalls
495 recalls tagged with “suffocation risk”.
Philips IntelliVue MX100 Patient Monitors Recalled for Alarm Failure (Z-0861-2026)
Potential issue where the IntelliVue monitors did not alarm.

Werner Paddles Recalls Stealth & Covert Kayak Paddles Over Drowning Hazard (2025)
This recall involves models Stealth and Covert kayak paddles. The brand name Werner appears on decals on both blades and the model name is printed on the right paddle blade. The paddles are made of black carbon fiber.

Grundens Recalls Youth Clipper 282 and Zenith 282 Jackets Over Drawstrings Strangulation Hazard (202

Modera Pack N Play Mattress Recall for Entrapment Risk in 2025
Modera recalled its Pack N Play Play Yard Mattresses sold at multiple retailers after a potential entrapment risk. The products may not fit play yards properly, creating dangerous gaps. Stop using the recalled mattresses and contact Modera for a full refund.

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025
Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.

WLIVE Fabric Drawer Dressers Recall Expanded to 16-Drawer Models for Tip-Over Hazards (2025)

HOMEAL Bed Rails Recalled for Entrapment Risk in 2025
HOMEAL bed rails sold on Amazon are recalled after entrapment risk was identified. The recall applies to HOMEAL-branded children’s bed rails with Model No. 338. Consumers should stop using the product immediately and contact HOMEAL for a full refund.

Harppa 5-in-1 Convertible High Chair Recall Expands Over Risk of Fall and Entrapment Hazards (2025)
B. Braun Medical Recalls 12,700 ADDitIV Gravity IV Sets Over Backflow Risk (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B. Braun Medical IV Administration Set Recall for 45,288 Units Over Backflow Risk (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical Recalls 12,168 IV Administration Sets for Backflow and Occlusion Risk (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical IV Administration Set Recall Affects 41,976 Units Worldwide (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical IV Administration Set Recall for 41,016 Units Over Backflow and Occlusion Risk (2025
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Vista IV Set Recall for 74,652 Units Over Backflow and Occlusion Risk
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical IV Administration Sets Recall Over Backflow and Occlusion Risk (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B. Braun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical IV Set Recall Affects 32,436 Units Over Backflow and Occlusion Risks (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
BBraun Medical Inc. Recalled 104,784 Anesthesia IV Sets Over Backflow, Occlusion Risk
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).