Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Medline recalled 4.4 million Quick Strip Plastic Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals compromising sterility. Consumers and healthcare providers should stop using these bandages immediately.
Medline Industries recalled 18,000 units of Curad Quick Strip Fabric Bandages on October 27, 2025. The recall affects all lots due to compromised seals that may affect sterility. Consumers should stop using these bandages immediately and follow recall instructions.
Medline Industries recalled 11,291,800 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals that compromise sterility. Consumers should stop using these bandages immediately.
Medline Industries recalled 1,725,600 units of Quick Strip Plastic Sterile Adhesive Bandages due to potential packaging defects. The recall, issued on October 27, 2025, affects all lots of Curad Touch-Free and Quick-Strip Bandages. Open seals may compromise the sterility of the product, posing a health risk.
Medline Industries recalled 1.57 million units of Curad Touch-Free and Quick-Strip Bandages on October 27, 2025. The packaging may exhibit open seals, compromising sterility. Consumers should stop use immediately and follow the recall instructions provided by the manufacturer.
Medline Industries recalled 6,989,900 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall stems from open seals in the packaging that may compromise sterility. Patients and healthcare providers should stop using these products immediately.
Philips North America recalled 110 Azurion 7 M20 interventional fluoroscopic X-ray systems on October 27, 2025. These devices were shipped without the necessary Source-to-Skin Distance (SSD) Spacer, violating FDA regulations. The absence of this spacer poses a serious health risk during fluoroscopy applications.
Whatcom Blue Sliced Cheese was recalled on October 27, 2025, due to potential E. coli contamination. The recall affects 411 lbs of cheese sold at Whole Foods Market in Washington and Oregon. Consumers should not consume the product and seek a refund or replacement.
Siemens Medical Solutions USA recalled one MAMMOMAT Fusion operator table on October 24, 2025. The table was sold with a bus-installation kit but is intended for stationary use only. This recall affects distribution in Arkansas, California, New York, and internationally in Australia, Canada, and India.
Water Pure recalled 17,612 bottles of My Bladder dietary supplement on October 24, 2025. The product may be contaminated with E. coli O7:K1 and E. coli 1303. Consumers should stop use immediately and seek refunds.
EDAN recalled 3,824 Patient Monitors on October 24, 2025. The recall follows an FDA letter regarding cybersecurity vulnerabilities. Affected models include X8, X10, and X12, distributed nationwide and to Mexico.
EDAN recalled 3,141 patient monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The recall affects models iM8, iM8A, and iM8B used for monitoring physiological parameters. Healthcare providers must stop using these devices immediately and follow the manufacturer's instructions.
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.
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 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.
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.
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.
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 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 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.