All Product Recalls

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

EDAN Recalls Patient Monitors Due to Cybersecurity Risks

EDAN recalled 342 patient monitors on October 24, 2025, due to potential cybersecurity issues. Models affected include elite V5, elite V6, and elite V8. Healthcare providers and patients should stop using these devices immediately.

EDAN Fetal Monitors Recalled Due to Cybersecurity Risk

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

GE Medical Systems Recalls Mammography Systems Over Labeling Hazard

GE Medical Systems recalled 1,818 Senographe Pristina mammography systems on October 24, 2025. The recall affects systems due to missing or incorrect X-Ray Warning labels. This nonconformance to FDA regulations poses a high hazard risk.

EDAN Telemetry Transmitter Recalled Over Cybersecurity Concerns

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

EDAN Recalls Fetal & Maternal Monitors Over Cybersecurity Risks

EDAN recalled 3,518 fetal and maternal monitors on October 24, 2025, due to potential cybersecurity issues. Affected models include F6, F9, F6 Express, and F9 Express. The recall impacts devices distributed in the U.S. and Mexico.

Sauna360 Recalls Tylö Halmstad and Kiruna Hybrid Saunas Over Fall Hazard

Cranach Hardware Recalls Tip Restraint Kits for Tip-Over Hazard (2025)

Olympia Tools Recalls Pack-N-Stroll Premium Folding Utility Wagon for 2025 Entrapment and Falls Risk

Bio Ionic 1-Inch Curling Iron Recalled for Burn Hazard (2025)

Bio Ionic recalls the 1-Inch-Long Barrel Curling Iron model LXT-CL-1.0 with date code 0722-1223. The recall is active as of 2025-10-23. Consumers should stop using the recalled curling iron and contact Bio Ionic for a free replacement.

LEACHOI Adult Portable Bed Rails Recalled for Entrapment Risk (2025)

LEACHOI recalled its adult portable bed rails sold on Amazon on Oct. 23, 2025. The recall covers ASIN B0BZVCG2R5 due to a risk of entrapment and suffocation and missing hazard labels. Stop using the recalled rails and seek a full refund from LEACHOI.

Bealife 5-Drawer Dressers Recalled for Tip-Over Hazard in 2025

Scepter B62 Dual-Chamber Fuel Containers Recalled for Fire and Child Poisoning Risk (2025)

Scepter B62 Dual-Chamber Fuel Containers Recalled for Flash Fire and Child-Poisoning Risk (2025)

3M Scotch TL909-50 Thermal Laminator Recalled for Overheating

Lifepro Bioremedy Infrared Sauna Blankets Recalled for Burn Hazard (2025)

Olympus Thunderbeat Surgical Instrument Recalled Due to Safety Concerns

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Surgical Instrument Recalled Due to Hazards

Olympus Corporation recalled 3,381 units of the Thunderbeat surgical instrument on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using the product immediately.

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Surgical Device Recalled Due to Adverse Events

Firm is initiating a removal due to continued reports of adverse events.