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
Corin Ltd recalled 3 Unity CR Femur knee implants due to labeling errors. Size 6 implants from batch 529803 may be labeled as size 7, and vice versa.
Cepheid is recalling Xpert Xpress Strep A test kits because pipettes may fail to dispense adequate sample volume, potentially resulting in invalid or absent test results.
Randox Laboratories is recalling the RX Daytona Plus (without ISE) IVD Clinical Chemistry Analyzer due to a flaw in rerun settings that may cause incorrect test result reporting.
Cosmedent is recalling the FlexiCup Composite Finishing & Polishing System due to reports that the elastomer cup material is crumbling. Approximately 7,400 packs distributed worldwide are affected.
Nature's Path Organic Dark Chocolate Chip Waffles are recalled because peanuts were not declared on the label, posing a risk to consumers with peanut allergies.
GlaxoSmithKline is recalling TUMS antacid tablets in Lot KH5L due to glass mineral wool contamination. Affected consumers should stop use immediately.
Corin Ltd is recalling Unity Total Knee System inserts due to a labeling mix-up between batches 529803 and 532405, potentially affecting size 6 and size 7 designations.
Nova Biomedical's Stat Profile Prime Plus POC analyzer may report inaccurate creatinine results during the first 2-4 hours after sensor cartridge installation. Standard quality control checks may not detect these errors.
TUMS Antacid chewable tablets (Assorted Berries, 1000 mg, lot HR5W) are being recalled nationwide because some bottles contain glass mineral wool. Consumers should stop using affected bottles immediately.
Sun Pharmaceutical is recalling approximately 2,304 bottles of Liothyronine Sodium Tablets, USP, 25 mcg (lot DNC2204A) due to failed impurity and degradation specifications. The affected medication was distributed nationwide.
Padagis US LLC is recalling Gynazole 1 butoconazole nitrate vaginal cream nationwide due to a manufacturing error where hydrophilic colloidal silica was used instead of hydrophobic colloidal silica.
Nature's Path Organic Pumpkin Spice Waffles are being recalled due to undeclared peanut allergen. About 6,908 cases were distributed across 17 states.
RayCare oncology information system versions 5B and 6A contain a software bug where document field values do not display when documents are opened in read-only mode outside the Documents workspace.
Pepsi Beverages is recalling Crush Orange Soda 24-packs due to plastic foreign material found in some cans. The recall affects 184 cases distributed in Minnesota with lot code JUL2924XXXXMC10243 and a best-by date of July 29, 2024.
Certain 2023 Ford F-250, F-350, and F-450 trucks with the Pro Trailer Hitch Assist feature may not display the rearview camera image, reducing rear visibility and increasing the risk of a crash.
GlaxoSmithKline is recalling TUMS Antacid (1000mg Calcium Carbonate) due to the presence of glass mineral wool. The affected lot (HV6B) was distributed nationwide.
Prevost is recalling 2022-2024 H3-45 and H3-45 VIP vehicles because the right front turn signal light may fail when activated. Inoperative turn signals and hazard lights reduce visibility to other drivers and increase crash risk.
Gulf States Toyota is recalling 195 2023 Toyota RAV4 vehicles equipped with 17" black alloy wheels. The tire valve stems may be improperly installed or damaged, potentially causing air leakage, underinflation, and crash risk.
Toyota and Subaru are recalling certain 2023 BZ4X and Solterra vehicles because hub bolts on the wheels may loosen and cause wheels to detach. Detached wheels can result in loss of vehicle control and crash risk.
General Motors is recalling certain 2022 Cadillac XT6, XT5, and GMC Acadia AWD vehicles due to a faulty fuel tank rollover valve that may not seal properly during a rollover crash, posing a fire risk.
Toyota is recalling certain 2022 Tundra and Tundra Hybrid vehicles due to loose axle shaft flange nuts that can separate from the axle housing. This separation can reduce vehicle stability and brake performance, increasing crash risk.
Honda is recalling certain 2020-2022 GL1800 Gold Wing motorcycles with manual transmissions due to a software error that may cause engine stalls. Engine stalls while riding can increase the risk of crashes.
Kia is recalling certain 2021-2022 Sorento Hybrid vehicles because the front seat belt pretensioners may explode in a crash, projecting metal fragments that could injure occupants. Dealers will secure the pretensioners with a cap at no cost.
Navistar is recalling certain 2022-2023 IC BUS school buses. The steering wheel retaining nut may have been tightened incorrectly, allowing the steering wheel to loosen or detach. Owners should not drive their vehicles until repaired.
Certain 2023 Jeep Grand Cherokee and 2022 Grand Cherokee 4XE vehicles may be missing the required air bag warning label. The missing label could prevent occupants from understanding proper restraint usage, potentially increasing injury risk in a crash.