2,153 recalls tagged with “stop use immediately”.
EDAN recalled 12,201 Vital Signs Monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected M3A model poses a high risk to patient safety by compromising monitoring accuracy. Users must stop using the devices immediately and follow recall instructions.
EDAN recalled 13,934 M3 Vital Signs Monitors on October 24, 2025 due to potential cybersecurity issues. The recall affects devices distributed in multiple U.S. states and Mexico. Healthcare professionals must stop using the device immediately and follow manufacturer instructions.
EDAN recalled 136 vital signs monitors on October 24, 2025, due to potential cybersecurity issues. The devices include models iM3s, iM3As, iM3Bs, and iHM3s. Patients and healthcare providers must stop using these monitors immediately and follow recall instructions.
EDAN recalled 11,987 iM3 Vital Signs Monitors on October 24, 2025 due to potential cybersecurity risks. The recall affects devices distributed across the United States and Mexico.
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.
Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.
Invagen Pharmaceuticals recalled Lanthanum Carbonate chewable tablets on October 24, 2025, due to stability issues. The tablets failed hardness specifications, posing a high hazard level. Healthcare providers and consumers should stop using the product immediately.
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.
One unit of the Siemens MAMMOMAT Fusion operator table is recalled after being sold with a bus-installation kit. The device is not intended for bus installations and is designed for stationary operation. Health care providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement sold nationwide after an FDA notice cited possible contamination with E. coli O7:K1 and E. coli 1303. The contamination could cause illness. Consumers should not consume the product and should contact Water Pure for refund or replacement information.
EDAN recalled 1,457 iT20 telemetry transmitters on October 24, 2025, due to potential cybersecurity issues. The recall affects devices distributed in the United States and Mexico. Healthcare providers and patients must immediately discontinue use of the device.
EDAN recalled 195 units of its Central Monitoring System MFM-CMS on October 24, 2025, due to potential cybersecurity issues. The recall follows an FDA letter warning about vulnerabilities that could impact device functionality. Users must stop using the device immediately and follow the manufacturer’s instructions for a remedy.
EDAN recalled 377 iM20 Patient Monitors on October 24, 2025, due to cybersecurity issues. The recall affects devices distributed nationwide in the U.S. and Mexico. Healthcare providers must stop using this device immediately.
EDAN recalled 3,721 fetal monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected models, F2 and F3, are used to monitor pregnant women and fetuses after 28 weeks of gestation. Healthcare providers must stop using these devices immediately and follow recall instructions.
EDAN recalled 14,550 Patient Monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected models include iM50, iM60, iM70, and iM80. Healthcare providers should stop using these devices immediately and follow the manufacturer's instructions for remedy.
Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek a full refund.
3M and its Scotch brand recalled the TL909-50 thermal laminator sold at Office Depot, Office Smart and School Specialty from August 2024 through September 2025. The units may overheat, creating a burn hazard. Consumers should stop using the recalled laminator, unplug it and contact 3M for a full refund.
Sauna360 recalls Tylö Halmstad and Kiruna Hybrid saunas sold by Sauna360 distributors nationwide from July 2024 through December 2024 for between $6,000 and $12,000. The recall targets bench seating that can collapse, creating a fall hazard. Stop using the benches immediately and contact Sauna360 for a free repair.
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.
Lifepro Fitness recalls Bioremedy Infrared Sauna Blankets sold with gray-faced controllers due to burn risk. The recall affects models LP-BRMDYL-BLK, LP-BRMDYL-GRY, LP-BRMDYR-BLK, LP-BRMDYR-GRY, LP-BRMDYR-BLU, LP-BRMDYR-PNK, and LP-BRMDYR-PRPL. Consumers should stop using and unplug the blankets and visit Lifepro’s recall page for a replacement.