Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Italian Parsley manufactured by MAYEJ COMERCIALIZADORA has been recalled nationwide due to contamination with Cyclospora cayetanensis. Consumers should not consume the affected product and should consult a healthcare provider if they have health concerns.
FDA recalls Philips Tempus Pro Patient Monitors because intracranial pressure and bladder pressure measurements have not been tested or validated for accuracy. Healthcare providers using unvalidated measurements could make incorrect clinical decisions.
Rovira snack crackers have been recalled because they contain undeclared FD&C Yellow #6 and Red 40 colorants not listed on product labels.
Integra LifeSciences is recalling the Codman Microsensor Basic Kit due to potential corrosion stains on the included 14-gauge Tuohy Needle. This device is used for intracranial pressure monitoring and corrosion could affect its function.
Philips Incisive CT scanners may produce incomplete scans due to an unstable connection inside the floating sensor. Healthcare facilities should not operate affected devices until repair is arranged with the manufacturer.
Sophysa is recalling 105 units of the Pressio 2 ICP Monitoring System due to customer complaints of unexpected rebooting. The malfunction could interrupt critical patient monitoring.
Siemens LUMINOS Lotus Max and dRF Max fluoroscopy systems with software version VF11 may display incorrect collimation when rapidly switching between organ programs. The defect affects devices with bucky wall stands for mobile detectors.
Fresh & Ready Foods recalls Spicy Egg Potatoes Cheese Tacos due to potential foreign material. 62 units with lot code LPK1WA336 were distributed in Oregon and Washington.
Sysco Imperial Potato Tater Barrel frozen potatoes are being recalled due to the presence of clear hard plastic fragments. Affected consumers should not consume the product and should discard it immediately.
Town Food Service aluminum sauce pans in 1QT to 3QT sizes are being recalled because they contain leachable lead. Approximately 11,300 units have been distributed across the United States, Puerto Rico, and Canada.
EverRoast Chicken Caesar Salad (8.5 oz, UPC 850042244142) with best-by dates from November 9-22, 2025 is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Kentucky and Indiana.
Fresh & Ready Foods is recalling 278 units of Spicy Veggie Breakfast Burritos distributed in Oregon and Washington due to the presence of foreign material. Consumers should not eat the affected product.
McCain Foods USA Inc is recalling 21,256 cases of Ore-Ida Tater Tots shaped potatoes due to the possible presence of clear hard plastic fragments. Consumers should not consume the product.
Waterfront Bistro brand frozen raw shrimp may be contaminated with Cesium-137. The recall involves approximately 1,800 cases.
Meijer Inc. is recalling Meijer Steam Distilled Water (128 FL OZ bottles, UPC 041250841197) due to floating black foreign substance found in the product. Lot Code 39-222 #3 distributed to Illinois, Indiana, Kentucky, Ohio, Michigan, and Wisconsin.
Rovira Tempting Crackers contain undeclared FD&C Yellow #6 and Red 40. Affected products are distributed across multiple U.S. states and territories. Consumers avoiding artificial colors should not consume these products.
AvKARE is recalling Rosuvastatin 10 mg tablets (Lot #49124) distributed nationwide because the tablets do not dissolve at the required rate, which may affect medication efficacy.
Imprimis is recalling intraocular injection products due to glass-like particles found in specific lots. The contamination poses a risk to eye health for patients receiving these injections.
A software issue in the BD Pyxis ES Enterprise Server may prevent timely updates of patient and medication information. The defect affects 2,079 systems distributed nationwide and in Canada and Bermuda.
Applied Medical Resources is recalling 450 units of Kii Low Profile surgical instruments due to a potential blade obturator assembly defect that could affect surgical performance.
Medline Hudson RCI oxygen masks may experience tubing disconnection during use, potentially delaying patient care and causing hypoxia. The company has received multiple complaints about this defect.
The HFD100 Head Fixation Device's torque screws may crack or separate during surgical use, potentially compromising head stabilization. IMRIS is recalling 122 affected units distributed worldwide.
Philips patient monitors may fail to reconnect to associated devices when moving between wireless access points with rapidly changing signal strength, potentially interrupting patient monitoring.
MARKET 32 by Price Chopper brand frozen raw shrimp may be contaminated with Cesium-137. The product was distributed in Connecticut, Massachusetts, New Hampshire, New York, Pennsylvania, and Vermont.
Imprimis NJOF is recalling Tri-Moxi intraocular injection due to glass-like particles found in certain lots. These particles could pose a risk to eye safety if injected.