Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Folsom Metal Products recalled 2,700 units of distraction pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Patients and healthcare providers must stop using the product immediately.
Folsom Metal Products recalled 3,790 distraction pins on August 21, 2025. The recall affects all lots distributed from August 1, 2020, to July 30, 2025. The labeling lacks a validated shelf life, posing a high hazard risk.
Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance reflecting updated sample types and measurement ranges. Healthcare providers must stop using the device immediately and follow recall instructions.
IBC Technologies recalled CX Combi Boilers on August 21, 2025, due to a burn hazard. The defective models can exceed safe hot water temperatures. Consumers should stop using the affected units immediately.
Abbott Point Of Care recalled 547,250 i-STAT EG6+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance for updated sample types and measurement ranges. Healthcare providers and patients must stop using these cartridges immediately.
Folsom Metal Products recalled 490 units of its 16 mm distraction pin on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Patients and healthcare providers must stop using the device immediately.
Folsom Metal Products recalled 160 units of distraction pins due to unvalidated shelf life labeling. The recall affects devices distributed across multiple states, including California and Texas. Patients and healthcare providers should stop using the product immediately.
Folsom Metal Products recalled 10 double packs of 14 mm Distraction Pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Healthcare providers and patients must stop using these devices immediately.
Taylor Farms recalled 8,284 units of its Honey Balsamic Salad Kit on August 21, 2025. The recall stems from undeclared allergens including sesame and soy. Consumers should not consume the affected products and seek refunds or replacements.
Abbott Point Of Care recalled 8,962,450 i-STAT CG8+ cartridges on August 21, 2025. The recall affects cartridges lacking proper 510(k) premarket clearance for updated sample types. Patients and healthcare providers must stop using these devices immediately.
Latitude 36 Foods recalled 46,800 units of Honey Balsamic dressing on August 21, 2025. The dressing contains undeclared soy and sesame, posing a serious health risk. Consumers should not consume the product and seek a refund.
Abbott Point Of Care recalled 6,115,950 i-STAT EG7+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance for updated measurement ranges. This issue affects the accuracy of potassium and ionized calcium tests, posing a high risk to patients.
Medline Industries recalled 828 units of catheter kits on August 21, 2025, due to potential shape retention issues. The affected products include Model Numbers DYNJ0415366P and DYNJ0415366Q. This recall poses a serious risk to patient safety.
Bard Peripheral Vascular recalled 1,725 Venclose digiRF Generators on August 21, 2025. The recall stems from software version 3.35 generating false positives for catheter defects. This issue can lead to improper device functionality during clinical use.
Major Pharmaceuticals recalled 26,628 cartons of Carvedilol Tablets on August 20, 2025. The recall stems from N-Nitroso Carvedilol Impurity-1 levels exceeding FDA limits. Consumers should stop using the product immediately and consult their healthcare provider.
Jessie's Lemon Meringue Pie is recalled due to undeclared Yellow#5. The recall affects over 136,000 units distributed across 13 states. Consumers should not consume the product and seek refunds.
Itacate Foods recalled 566 packages of CHARGE-UP CHILAQUILES on August 20, 2025. The product contains undeclared Yellow #5 and Yellow #6, posing a health risk. Consumers should not consume the product and seek a refund or replacement.
Abiomed recalled 71 Automated Impella Controllers on August 20, 2025. The devices may fail to perform correctly, leading to pump stoppage. Healthcare providers and patients must stop using these devices immediately.
Hostess recalled 60,630 cases of Ding Dongs on August 20, 2025, following reports of mold contamination. The recall affects various packaging sizes sold across multiple states. Consumers should not consume the product and seek refunds or replacements immediately.
Northwind Pharmaceuticals recalled Sulfamethoxazole and Trimethoprim Tablets on August 20, 2025. The recall affects several lot numbers due to a foreign substance found in packaging. Consumers should stop using the product and seek guidance immediately.