lithium battery Recalls
262 recalls tagged with “lithium battery”.


Peloton Recalls Original Series Bike+ Exercise Bikes Over Seat-Post Fall Hazard (2025)

GET TESTED INTERNATIONAL AB Hair Mineral Analysis Recall 19 Units (2025)
Distribution without premarket approval/clearance.
Get Tested International AB 3 in 1 STI Test Recalled for Premarket Approval Issue (2025)
Distribution without premarket approval/clearance.

Knog Blinder 900 and Blinder 1300 Bike Lights Recalled for Fire Hazard (2025)
B. Braun Medical Extension Set Recall Covers 300 Units for Backflow, Occlusion Risk (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 Recall Affects 2,544 Units Worldwide
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: 5,100 Units Distributed Worldwide Over Backflow and Oc
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Siemens MAMMOMAT Fusion Operator Table Recalled for Bus-Installation Risk (2025)
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
Water Pure My Bladder Recall for E. coli Contamination — 17,612 Bottles (2025)
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

Lifepro Bioremedy Infrared Sauna Blankets Recalled for Burn Hazard (2025)
Mindray Sevoflurane V90 Vaporizer Recalled for Leakage Risk in A9 System (148 Units)
Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.
M.C.I. Foods Recalls 1,040 Cases of Ready-to-Eat Egg & Cheese Breakfast Burritos and Wraps (2025)
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
