These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Pacific Coast Producers recalled 1,836 cases of canned pears on September 4, 2025, due to potential lead contamination. The affected product includes pears in pear juice concentrate sold in 15-ounce cans. Consumers should not consume the product and seek refunds immediately.
American Contract Systems recalled 32,433 biopsy trays on September 4, 2025. The recall affects multiple models due to improper re-sterilization that raises safety concerns. Healthcare providers and patients must stop using these products immediately.
Good and Gather recalled 57,240 bags of Southwest-Style Burrito Bowl Blend on September 4, 2025. The product may contain undeclared shrimp, posing a serious risk to those with shellfish allergies. Consumers should not consume the product and contact ONE FROZEN for refunds or replacements.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards after being re-gassed improperly. Health providers and patients must stop using these devices immediately.
Lutronic recalled 7,490 units of the XERF EFFECTOR 60 electrosurgical unit on September 4, 2025. Manufacturing defects may lead to adverse events for patients. Devices manufactured between April 1, 2025, and August 20, 2025, are affected.
American Contract Systems recalled 32,433 medical convenience kits after multiple sterilization cycles compromised product safety. The recall, announced on September 4, 2025, stems from nonconformance during Ethylene Oxide gas sterilization. Affected products include kits used for cataract and eye procedures.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows issues with multiple sterilization cycles that compromise product safety. Patients and healthcare providers should stop using these devices immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025, after discovering re-gassing issues. The affected products have not been validated for safety and effectiveness after multiple sterilization cycles.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. These kits failed to meet safety standards due to improper sterilization processes. The recall affects multiple states, including South Dakota and Iowa.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows the identification of products that were re-gassed after sterilization failures. The safety and effectiveness of these products cannot be confirmed due to multiple sterilization cycles.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall stems from products being re-gassed after a nonconformance during sterilization. This compromises the quality and safety of the devices.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards, posing a safety risk. Healthcare providers and patients must stop using these kits immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall affects various models due to improper sterilization processes. Patients and healthcare providers must stop using these products immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025, due to improper sterilization. The affected products were re-gassed and not validated for safety after multiple sterilization cycles. Distribution occurred nationwide, including states such as South Dakota and Illinois.
Organicare Nature's Science recalled 15,075 bottles of FemiClear Daily Bladder Strength Dietary Supplement on September 4, 2025. The recall stems from microbial contamination with E. coli O7:K1 and E. coli 1303. Consumers should not consume the product and seek refunds immediately.
Wegmans Food Markets recalled 102 cases of halved pears in pear juice on September 4, 2025. The recall follows concerns of potential lead contamination. Consumers should not consume the product and seek refunds.
Wegmans Food Markets recalled 609 cases of Fruit Cocktail on September 4, 2025, due to potential lead contamination. The affected product includes diced peaches and pears, distributed across multiple states. Consumers should not consume the recalled product and seek a refund or replacement.
Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane systems on September 3, 2025. The recall affects units distributed globally due to potential failures in internal components. If malfunction occurs, motorized movements will be disabled, posing risks to operational efficiency.
Endico Potatoes Inc recalled 280 cases of mixed vegetables on September 3, 2025. The frozen product may be contaminated with Listeria monocytogenes. It was distributed in New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland, and Washington, D.C.
Philips Medical Systems recalled 286 Allura Xper FD10/10 imaging systems on September 3, 2025. The recall affects models 722011, 722027, and 722005 due to potential failure of internal components. This malfunction could inhibit motorized movements, posing risks to patient safety.