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
Clarus Medical recalls the Lase Discectomy Device Kit due to potential compromise of the sterile barrier seal. Approximately 858 units were distributed in the US and internationally.
Cardiovascular Systems Inc is recalling STEALTH 360 GEN2 peripheral atherectomy devices due to potential mislabeling of crown sizes. Some 1.50mm crowns may be labeled as 1.25mm and vice versa, potentially affecting device performance.
Aspen Surgical Products is recalling 124 Norton Arm Kits due to bioburden levels exceeding sterilization validation limits, creating potential risk of surgical site infection.
Your Way Fresh Greek Yogurt + Peach Parfait is being recalled because soy lecithin in an ingredient is not declared on the label, posing a risk to consumers with soy allergies.
Mai Cuisine is recalling 12 PC Shrimp Tempura Kabuki Roll products sold at Genji Sushi counters in Whole Foods Market stores in Northern California due to Salmonella contamination in the frozen shrimp used in these products.
DePuy Orthopaedics' TruMatch CT surgical instrument system has a software coding error that may prevent proper alignment of scanning images, potentially causing limb malalignment during joint replacement surgery.
Mai Cuisine is recalling Shrimp California Roll products sold at Genji Sushi counters in Whole Foods Market stores in Northern California due to Salmonella contamination in the frozen shrimp ingredient.
Smiths Medical ASD Inc. is recalling 1,590 units of Smiths Medical Portex Tracheal Intubation Stylets because incorrect devices were found in packages. The affected lot was distributed internationally.
Mai Cuisine is recalling Cooked Variety Pack sushi products sold at New Leaf Community Market stores in Northern California due to Salmonella contamination in frozen shrimp used in the products.
Elekta's Monaco RTP System software (builds 5.40.00, 5.40.01, 5.40.02, 5.51.10) may calculate incorrect radiation doses if a treatment couch is removed and reinserted during specific plan loading operations.
China Gel Inc is recalling China-Gel (menthol and camphor) topical pain reliever products due to contamination with B. cepacia found in the manufacturing facility where the product was made.
Mai Cuisine is recalling sushi products sold at Genji Sushi counters in Northern California Whole Foods Markets due to Salmonella contamination in frozen shrimp used as an ingredient. Products with hand-crafted dates of 8/12/2021 or 8/13/2021 are affected.
Forest River is recalling certain 2021 Berkshire recreational vehicles that may have unsealed mini-breakers in the electrical system, which could cause sparks and increase the risk of fire in the battery compartment.
Forest River is recalling 2021-2022 Coachmen Nova motorhomes because the Absorbed Glass Mat battery was incorrectly installed, allowing hydrogen gas to accumulate inside the vehicle and create a risk of injury.
Starcraft is recalling certain 2021-2022 recreational vehicles with defective Winntec propane regulators that may fail, causing increased pressure and larger flames in gas appliances, raising fire risk.
The Step2 Company is recalling StepUp Sidekick Learning Towers because the storage tray with cup holders and step can come loose, posing a fall hazard to children. Step2 has received 20 reports of the component coming loose, including one report of minor bruises from a fall.
Certain 2018-2021 Toyota Tundra vehicles have a headlight electrical circuit defect that may power high and low beams simultaneously, causing connector overheating and fire risk. Owners should contact Toyota or NHTSA for remedy information.
Daimler Trucks North America is recalling 2019-2021 Freightliner Cascadia trucks due to improperly tightened drag link taper joints that could separate from the steering arm. Loss of steering control could result, increasing crash risk.
Jayco is recalling certain 2017-2022 recreational vehicles with Winntec propane regulators that may fail and increase propane pressure, raising the risk of fire in gas appliances.
Cardinal Health recalls 267 million Monoject 0.9% Sodium Chloride Flush Syringes due to a plunger defect that may reintroduce air into the syringe, posing a risk of air embolism during IV administration.
Cardinal Health Monoject flush syringes may have a defect allowing the plunger to draw back and reintroduce air into the syringe. The FDA issued a Class I recall for over 267 million units distributed nationwide.
Eli Lilly & Company is recalling Trulicity (dulaglutide) 0.75 mg autoinjector pens because some contain double the labeled strength. Affected patients may receive an incorrect dose.
HIS ENTERPRISE INC is recalling all lots of Miss Slim capsules (10-count and 30-count boxes) distributed nationwide in the USA because the product was marketed without required FDA approval (ANDA/NDA).
Cahills Farm Cheese Limited is recalling Lidl Preferred Selection Red Wine Cheddar cheese due to potential Listeria monocytogenes contamination. Consumers should not eat this product.
SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection (1,000 mL bags) nationwide due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider immediately.