2,756 recalls tagged with “immediate action”.
Moonlight Packing Corporation recalled over 102,000 cases of yellow peaches on October 28, 2025. The recall follows potential contamination with Listeria monocytogenes. The affected peaches were distributed across multiple U.S. states and in Canada and Mexico.
Potential contamination with Listeria monocytogenes.
Potential contamination with Listeria monocytogenes.
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
Moonlight Packing Corporation recalled 237,656 cases of yellow peaches on October 28, 2025, due to potential Listeria monocytogenes contamination. The recall affects multiple states across the U.S. and extends to Canada and Mexico.
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 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 has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Screw may loosen or fallout of Hemodialysis system
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 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.