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.
Deep-brand PREMIUM Select Fansi Cut French Beans have been recalled after testing positive for Salmonella. The recall affects approximately 3,509,532 bags distributed across the United States. Consumers should not consume the product and seek a refund immediately.
CHETAK NEW YORK recalled over 3.5 million bags of Premium Select Amla Slices on September 5, 2025, after testing positive for Salmonella. Consumers should not consume this product and seek refunds or replacements. The recall affects various lot numbers sold across the United States.
Chetak New York recalled over 3.5 million bags of frozen Tindora on September 5, 2025. The recall follows positive tests for Salmonella, a bacteria that can cause serious illness. Consumers should not consume the product and seek a refund or replacement immediately.
Chetak New York LLC recalled over 3.5 million bags of Deep-brand Select Val Papdi on September 5, 2025, after testing positive for Salmonella. The recall affects various lot numbers, prompting an immediate stop to consumption and a request for refunds or replacements.
Spacelabs Healthcare recalled 820 DVI display cables on September 5, 2025. The cables may interfere with other medical devices due to inadequate shielding. Patients and healthcare providers should stop using these cables immediately.
Deep-brand Premium Select Karela Ring Cut recalled over Salmonella contamination. The recall affects 3,509,532 bags sold in the U.S. Consumers should not consume the product.
Chetak New York LLC recalled over 3.5 million bags of frozen baby bhindi on September 5, 2025, due to potential Salmonella contamination. The recall affects the Deep-brand Premium Select Baby Bhindi, weighing 12 oz. Consumers should not consume this product and seek refunds immediately.
Apotex Inc. recalled 151,034 bottles of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution on September 5, 2025. The recall stems from a lack of assurance of sterility due to improper bottle sealing. Consumers should stop using the product immediately and contact their healthcare provider or Apotex Corp.
CHETAK NEW YORK recalled over 3.5 million bags of Dum Aloo on September 5, 2025, after testing positive for Salmonella. The recall affects products distributed throughout the United States. Consumers should not eat the product and seek a refund or replacement.
CHETAK NEW YORK recalled over 3.5 million bags of PREMIUM Select Lotus Root on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk. Consumers should stop using the product immediately and seek refunds.
CHETAK NEW YORK recalled 3,509,532 bags of PREMIUM Select Falsa KEEP FROZEN on September 5, 2025. The product tested positive for Salmonella, a serious health risk. Consumers should not consume the product and can contact the company for refunds.
URMYWO recalled baby loungers on September 4, 2025, due to suffocation and fall hazards. The loungers violate safety standards, posing risks of serious injury or death. Consumers should stop using the product immediately and contact Pomona for a refund.
StopBox USA recalled AR-15 Chamber Lock Pro firearm locks on September 4, 2025. A manufacturing defect allows unauthorized access to firearms, posing a risk of serious injury or death. Consumers should immediately stop using the locks and contact StopBox for refunds or replacements.
Zydus Pharmaceuticals recalled 4,440 bottles of Entecavir Tablets on September 4, 2025. The recall follows failure to meet impurity and degradation specifications. Consumers should stop using the affected tablets immediately and contact their healthcare provider.
Zydus Pharmaceuticals recalled 4,344 bottles of Entecavir Tablets on September 4, 2025. The recall stems from failed impurity and degradation specifications. Consumers should stop using the product immediately.
American Contract Systems recalled 32,433 radiology packs on September 4, 2025, due to improper sterilization. The products were re-gassed after a nonconformance in the initial Ethylene Oxide gas injection process. Their safety and effectiveness remain unverified after multiple sterilization cycles.
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.
Pacific Coast Producers recalled 2,436 cans of sliced pears on September 4, 2025. The canned pears may contain lead, posing a significant health risk. Consumers should not consume these products and follow the recall instructions immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The kits were re-gassed after a noncompliance during the Ethylene Oxide sterilization process. This raises concerns about their safety and effectiveness.
American Contract Systems recalled 32,433 Basic Biopsy Trays on September 4, 2025. The recall resulted from products being re-gassed after a sterilization failure. The company cannot confirm the safety or effectiveness of these devices after multiple sterilization cycles.