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
Fruit Fresh Up, Inc. is recalling Fresh Harvest Small fruit platters with raspberry dip due to potential Listeria monocytogenes contamination. The recall affects products distributed in NY, MA, and PA.
T Fresh Company is recalling Yes! Enoki Mushrooms due to Listeria monocytogenes contamination detected in samples. The product was distributed to California, Georgia, and Texas.
Fruit Fresh Up, Inc. is recalling Eden Valley Bulk Fruit Salad which may be contaminated with Listeria monocytogenes. The recall affects 39,232 units distributed in New York, Massachusetts, and Pennsylvania.
Fruit Fresh Up, Inc. is recalling Doodlebugs Tidbits Mix (cantaloupe, honeydew, pineapple, watermelon) distributed in New York, Massachusetts, and Pennsylvania due to potential Listeria monocytogenes contamination.
Tops Dill Dip Bulk is being recalled due to potential contamination with Listeria monocytogenes. Consumers should stop using the product and dispose of it safely.
Top Quality Produce Enoki Mushrooms are recalled due to Listeria monocytogenes contamination detected by California Department of Public Health. The recall affects 1108 cases distributed across six states.
Adamis Pharmaceuticals is recalling SYMJEPI epinephrine injections due to potential needle clogging that may prevent medication delivery. The FDA has classified this as a Class I recall affecting nationwide distribution.
Adamis Pharmaceuticals is recalling 2,500 cartons of SYMJEPI (epinephrine injection) nationwide due to a defective delivery system that may clog the needle and prevent medication dispensing.
Fruit Fresh Up, Inc. recalled watermelon products from multiple retailers due to potential Listeria monocytogenes contamination. The recall affects 39,232 units distributed in NY, MA, and PA with best-by dates of March 5–23, 2022.
Fruit Fresh Up, Inc. recalls honeydew products that may contain Listeria monocytogenes. Affected products with best-by dates 03/05/2022–03/23/2022 were distributed in NY, MA, and PA.
Fruit Fresh Up is recalling multiple pineapple products sold under various store brands due to potential Listeria monocytogenes contamination. Affected products were distributed in New York, Massachusetts, and Pennsylvania with best-by dates from March 5 to March 23, 2022.
Fruit Fresh Up, Inc. is recalling six cantaloupe products distributed in NY, MA, and PA (39,232 units) due to potential Listeria monocytogenes contamination. Products have best-by dates between March 5 and March 26, 2022.
Fruit Fresh Up, Inc. is recalling Fruit Fresh Up Raspberry Dip (7oz) due to potential Listeria monocytogenes contamination. Affected units distributed in NY, MA, and PA should not be consumed.
Melon trio and combo products from Fruit Fresh Up may contain Listeria monocytogenes. Products distributed in NY, MA, and PA with best-by dates from March 5–23, 2022 are affected.
Fruit Fresh Up, Inc. recalls MapleVale 18# Wet Salad Bucket due to potential Listeria monocytogenes contamination. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
Shimadzu SonialVision safire X-ray systems may emit radiation exceeding federal limits during some fluoroscopic procedures. The manufacturer is addressing installation criteria to prevent potential dose violations.
DeRoyal Industries is recalling 400 DeRoyal ST Neonatal Dressing Change Kits due to uncertain validation of manufacturing test methods. The recall affects kits distributed to healthcare facilities in Florida, New Jersey, and Tennessee.
Maquet Medical Systems is recalling certain Cardiohelp-i Transport Guard units due to a potential loose cylindrical pin that may jam the locking mechanism. This could prevent the device from opening or cause complete disassembly, potentially delaying critical cardiac support.
Ventana Medical Systems has recalled 9,214 BenchMark ULTRA and DISCOVERY ULTRA instruments due to potential fluid leak that could cause electrical short circuit, smoke, and fire.
Remote Diagnostic Technologies recalls Tempus LS defibrillators not approved for US distribution. Two units were distributed in Illinois and Kansas.
Tetracaine 1% Injectable is being recalled due to sterility assurance failures caused by manufacturing deviations that may compromise product sterility.
Forest River is recalling certain 2021–2023 recreational vehicles because quick disconnect fittings in the LP gas system may crack and leak, creating a fire risk in the presence of an ignition source.
Medline Industries is recalling 7,800 Excelsior Medical 10mL Sterile Field Saline Flush syringes due to sterility failure of the exterior syringe surface, which may prevent the product from being safely used on a sterile field.
Fruit Fresh Up, Inc. is recalling Fresh Harvest Small veggie platters with ranch that may be contaminated with Listeria monocytogenes. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
WHPM Inc. is recalling approximately 535,755 First SIGN SARS-CoV-2 Antigen Tests distributed in California, Florida, Louisiana, Massachusetts, and Texas. The tests were sold without FDA Emergency Use Authorization or clearance.