2,715 recalls tagged with “immediate action”.
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 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.
Sadecki Bartnik recalled 336 jars of bee pollen on September 4, 2025, due to detectable pyrrolizidine alkaloids. These compounds pose health risks if consumed. Consumers should stop using the product immediately and seek a refund.
Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects 10 mg tablets sold nationwide due to contamination with N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and consult healthcare providers.
Sun Pharmaceutical Industries recalled 1,870 kits of Technetium Tc 99m Mertiatide on September 3, 2025. The recall follows failed dissolution specifications for a key ingredient. The affected kits were distributed nationwide and pose a high risk to patients.
Zydus Pharmaceuticals recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects a specific lot due to contamination with N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Endico Potatoes Inc recalled 335 cases of frozen peas and carrots on September 3, 2025. The products may contain Listeria monocytogenes, a bacteria that can cause serious illness. The affected items were distributed in several states including New York and Florida.
Philips Medical Systems Nederland B.V. recalled five Biplane OR Tables on September 3, 2025, due to potential failure of internal components. The recall affects models 722020 and 722025, distributed worldwide. Users must stop using the affected devices immediately to avoid operational issues.
Philips Medical Systems Nederland B.V. recalled 174 OR tables on September 3, 2025. The recall affects models 722023, 722035, and 722015 due to potential failure of motorized movements. Users must stop using these devices immediately to prevent operational issues.
Philips Medical Systems Nederland B.V. recalled 98 radiology imaging systems on September 3, 2025. The recall stems from internal component deterioration that may hinder motorized movements. Patients and healthcare providers must stop using the devices immediately.
Philips Medical Systems Netherlands B.V. recalled three Allura Xper FD20/20 OR Tables on September 3, 2025. The recall addresses potential failures in internal components that could impede motorized functions. Users must stop using the device immediately and follow recall instructions.
Philips Medical Systems Nederland B.V. recalled 75 Allura Xper FD20/20 imaging systems on September 3, 2025. The recall affects systems due to internal component deterioration, which can hinder motorized movements. All users must stop using the device immediately and follow manufacturer instructions for safe handling.
Philips Medical Systems recalled 2,114 Allura Xper FD20 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, risking loss of motorized functionality. This recall affects 791 units in the U.S. and 1,323 globally.
Philips Medical Systems Nederland B.V. recalled two operating room tables on September 3, 2025. The recall affects models 722022 and 722033 due to potential system failures. The malfunction can inhibit motorized movements, posing a risk to patients and healthcare providers.
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.
Philips Medical Systems Nederland B.V. recalled 45 Allura Xper FD20/10 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, posing a high risk to users. Affected units include 11 in the U.S. and 34 internationally.
Philips Medical Systems Nederland B.V. recalled the Allura Xper FD20/15 OR Table on September 3, 2025. The recall affects one unit distributed worldwide, including the U.S. Systems may not perform as intended due to internal component deterioration.
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.
Zydus Lifesciences recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects tablets with NDC 16714-051-01 due to N-Nitroso Desmethyl Chlorpromazine exceeding acceptable limits. Consumers should stop using the product immediately and consult healthcare providers.