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 the agency’s own highest classification or reported deaths or serious injuries, 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
Baxter Healthcare is recalling the Welch Allyn Connex Spot Monitor due to improper placement of copper tape on the back of the liquid-crystal display. The device was distributed in California.
Twin Cities Co-Op Partners is recalling 720 containers of La Reyna Gluten Free Guacamole distributed to IA, MI, MN, and WI because the product was shipped at improper temperatures without quarantine.
Keystone Industries recalls Copaliner Cavity Varnish after discovering bottles of Copaliner Solvent were accidentally packaged in boxes labeled as varnish. The error affected 337 units distributed worldwide.
Landauer is recalling nanoDot D2DNS radiation monitoring dosimeters due to a potential defect in the OSL material. Affected devices may provide radiation exposure readings outside the specified +/-5.5% accuracy range.
Twin Cities Co-Op Partners is recalling 720 containers of La Reyna Salsa Roja due to temperature storage violations. The product was shipped to customers without proper quarantine after being stored outside required refrigeration specifications.
Twin Cities Co-Op Partners Inc. is recalling La Reyna Salsa Verde after the product was stored and shipped without maintaining proper temperature specifications.
Twin Cities Co-Op Partners is recalling 720 containers of La Reyna Queso Dip due to temperature control violations during shipment. The product was not quarantined after being received out of specification.
Keystone Industries is recalling 240 units of Henry Schein Hard Line Chairside Reline kits because the outer box is labeled as Soft Line, though the contents and instructions are correctly labeled.
Landauer is recalling 211,815 nanoDot D2DNS radiation dosimeters worldwide. Some units may be outside the specified ±5.5% accuracy range due to a defect in the optical material, potentially resulting in inaccurate radiation exposure measurements.
Twin Cities Co-Op Partners Inc. is recalling La Reyna Diablo Salsa because the product was received and shipped at improper temperatures. Refrigerated foods improperly stored may develop harmful bacteria.
Microbiologics Inc is recalling one lot of KWIK-STIK ANA QC sets missing one of three bacterial strains required for microbiological testing.
Advance Medical Designs is recalling ASG-001 ultrasound gel due to mislabeling of use instructions. The product was distributed in the US, Canada, UK, Panama, and Netherlands.
Advance Medical Designs is recalling 50-GEL20 ultrasound gel (13,750 units, lot 21043C2328) due to mislabeling with inappropriate use instructions. The product was distributed in the US, Canada, UK, Panama, and the Netherlands.
Advance Medical Designs is recalling procedural kits containing ultrasonic transmission gel because the product labeling does not accurately indicate appropriate use. The recall affects 460 units distributed to the US, Canada, UK, Panama, and Netherlands.
Hyundam Industrial is recalling fuel pumps where the impeller may deform, causing pump failure and loss of drive power, which increases the risk of a crash.
Certain 2022-2023 Jeep Wrangler and Gladiator vehicles with manual transmission have a defective gear position sensor that may prevent the rearview camera from displaying and the reverse lights from illuminating, creating a visibility and safety hazard.
Chrysler is recalling specific Mopar Gear Position Sensors and Transmission Assemblies because they may cause rearview camera and reverse light failures, increasing crash risk.
Chrysler is recalling certain 2023 Dodge Durango Pursuit vehicles because the shifter may slip out of gear while driving, causing sudden loss of drive power and increasing crash risk.
USDA FSIS issued a public health alert for specific Hormel SPAM Classic cans due to possible under-processing. Consumers should not eat the product.
American Foods Group is recalling approximately 58,281 pounds of ground beef products that may be contaminated with E. coli O103. The products were shipped to distributors in Georgia, Michigan, and Ohio.
Winnebago is recalling multiple 2020-2022 motorhome models due to an incorrect hitch label that can lead to vehicle overloading. Dealers will install the correct label at no cost.
Kia is recalling 2019 Sorento vehicles because water may leak into the rearview camera, preventing the image from displaying and increasing crash risk.
Forest River is recalling certain 2024 Palomino truck campers due to an unnecessary charge line connected to the lithium battery that may cause overcharging and fire risk. Dealers will disconnect the line and install bell caps free of charge.
Buffalo Games and Target are recalling Chuckle & Roar Ultimate Water Beads Activity Kits because ingested water beads expand and can cause choking and intestinal obstruction in children. One infant death and one serious injury requiring surgery have been reported.
Gillig is recalling 223 Low Floor transit buses from 2022-2023 because improperly tightened driveshaft fasteners could allow the driveshaft to detach, increasing crash risk.