
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.

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.

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.

HEB Recalls 12-Pack Destination Holiday Glow Light Stick Bracelets Over Skin Irritation Hazard (2025

Milwaukee Tool Recalls M18 FUEL 12" and 14" Top-Handle Chainsaws for Laceration Hazard (2025)

Polaris Recalls 2025-2026 Ranger XP 1000 NorthStar UTVs for Fire Hazard

Knog Blinder 900 and Blinder 1300 Bike Lights Recalled for Fire Hazard (2025)


WLIVE Fabric Drawer Dressers Recall Expanded to 16-Drawer Models for Tip-Over Hazards (2025)
B Braun Medical IV Administration Set Recall for 4,488 Units in 2025
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
BBMIs Infusomat IV Administration Set Recall, 63,192 Units Worldwide for 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 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 Administration Sets Recalled for Backflow Risk and Occlusion (2025)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Avion Pharmaceuticals Prenate Chewable Prenatal Vitamin Recalled for Undeclared Soy (804 Bottles, 5
Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.
B. Braun Medical SAFELINE IV Sets Recalled for 46,250 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 IV Administration Sets Recalled for Backflow and Occlusion Risk (490549, 490565)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical Recalls 19,104 IV Administration Sets for 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 15,250 PB1500 IV Set 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 29,900 Units Over Backflow and Occlusion Risk (202
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 2025 for Backflow and Occlusion Risk (490437)
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).