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
Forest River is recalling 2017 Dynamax DX3 and Force motorhomes because the front axle stabilizer bracket may break, increasing crash risk.
Keystone RV Company is recalling 2020 Dutchmen Atlas 3382BH trailers because a non-metallic propane hose may melt and leak gas, posing a fire risk.
MawMaw's Chicken Pies is recalling chicken pie and meatloaf products in North Carolina because they contain undeclared milk and soy allergens.
Hendrickson is recalling CONNEX ST steerable suspension and axle systems because mounting washers may fracture, potentially reducing braking ability and increasing crash risk.
T & R Enterprise USA Inc. is recalling approximately 126,000 pounds of meat and poultry egg roll products produced under insanitary conditions. The products were shipped to institutional locations in Georgia and Missouri.
Toyota is recalling approximately 928,220 vehicles because previously replaced airbag inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Halcore is recalling 2018-2019 Horton Type I and Type III ambulances because the oxygen tank bracket may loosen, allowing the tank to become airborne in a crash.
Voyager Industries is recalling 2018-2020 Yetti trailers because missing retainer clips may allow spindle nuts to loosen, potentially causing the wheel to come off the axle.
Global Zakii Enterprises is recalling 174 pounds of canned meat and poultry products imported from Jordan without required inspection.
Lipari Foods is recalling Premo and Fresh Grab chicken salad sandwiches after FDA environmental sampling detected Listeria monocytogenes.
Lipari Foods is recalling Fresh Grab Turkey No Cheese sandwiches after FDA testing detected Listeria monocytogenes. Consumers should discard or return the product.
Lipari Foods is recalling Premo and Fresh Grab Tuna Salad sandwiches after FDA environmental sampling detected Listeria monocytogenes.
Consider Bardwell Farm is recalling Experience Handmade Cow Cheese due to potential Listeria monocytogenes contamination. The product was distributed in six states.
Lipari Foods is recalling Premo and Fresh Grab Egg Salad sandwiches after FDA environmental sampling detected Listeria monocytogenes.
Sara Lee Frozen Bakery is recalling Chef Pierre Small Whole Grain Banana Muffins after a consumer reported finding tree nut foreign material in the product.
Consider Bardwell Farm is recalling Slyboro Handmade Goat Cheese because it may be contaminated with Listeria monocytogenes.
TriMed Inc. is recalling 5 Dorsal Wrist Hook Plates due to unqualified design modifications that may compromise structural integrity.
GCP Laboratories is recalling Major Infants' Gas Relief Drops due to microbial contamination of the non-sterile product.
Becton, Dickinson and Company is recalling 22 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with BD Trucount Tubes.
Sandoz is recalling 13,130 bottles of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.
Sandoz is recalling specific lots of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.
Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution because it failed impurity specifications for Prednisolone Impurity 14.
Lipari Foods is recalling Premo brand Bologna & Cheese Wedges because FDA environmental testing detected Listeria monocytogenes.
Porsche is recalling 2017-2020 Cayenne and Panamera vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out.
Unipharma is recalling DrKids Himasal Natural Nasal Saline Solution vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.