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
Bix Produce Company LLC is recalling diced spinach due to plastic contamination. The recall affects 1,181 cases distributed in Wisconsin with use-by dates between January and June 2022.
Arcoma AB is recalling 71 Omnera 400T radiographic systems because liquid ingress in the display handles may cause electrical short circuits and uncontrolled movement of the overhead tube crane.
Arcoma AB recalls 47 Omnera 400A Digital Radiographic Systems due to potential electrical short circuits that could cause uncontrolled movement of the overhead tube crane.
SoDelicious DairyFree Wondermilk Salted Caramel Sundae cones are recalled due to peanut contamination. Some cartons mistakenly contain peanut pieces, posing a serious risk to consumers with peanut allergies.
Cervasi Pecorino Romano Cheese is being recalled by Paris Brothers Inc due to Listeria contamination detected in environmental samples at the production facility.
Wedgewood Village Pharmacy is recalling Estriol 1mg/gm Vaginal Cream due to insanitary manufacturing conditions and lack of adequate processing controls identified during FDA inspection. The product was distributed nationwide.
Menarini Silicon Biosystems is recalling CELLSEARCH Circulating Tumor Cell Kit due to potential false positive results in patient samples. The device may generate unassigned events that could affect diagnostic accuracy.
Paris Brothers Inc is recalling Colby Jack Cheese due to environmental samples testing positive for Listeria. Affected product has lot code 05042022 and best-by date of August 3–4, 2022.
Siemens is recalling the Dimension LTNI cardiac troponin-I test due to positive bias in Lithium Heparin plasma samples, which may cause false-positive results and inappropriate medical intervention.
Milton Creamery Tomato Garlic Cheddar Cheese, made by Paris Brothers Inc, is being recalled because Listeria was detected in environmental samples. The affected product was distributed to wholesale warehouses, grocery stores, and food service establishments.
Chromsystems has recalled MassCheck Amino Acid, Acylcarnitines dried blood controls (batch 2821) for insufficient glycine concentration. This may affect laboratory test accuracy.
Paris Brothers Inc recalled Pepper Jack Cheese after environmental samples from the production facility tested positive for Listeria.
GE Centricity Universal Viewer Zero Footprint software can display inaccurate measurements on medical images. This Class II recall affects approximately 1,934 units distributed worldwide.
The FDA has recalled Boric Acid 600 mg capsules (Lot #000-03868160, Exp: 09/14/22) manufactured by Wedgewood Village Pharmacy due to insanitary conditions and lack of processing controls observed during FDA inspection. The recalled product was distributed nationwide.
Siemens Artis and Artis Q.zeego fluoroscopic X-ray systems may lose stand mobility if the robotic control system's BIOS battery discharges at startup. Field service is required to restore function.
Luminex Corporation is recalling the Verigene CDF Nucleic Acid Test due to potential false negative results caused by the swab's hydrophobic characteristics, which could result in missed positive diagnoses.
Vermeer is recalling 2022 BC1800XL trailers because improper hitch bolts may fail, causing the trailer to separate and increasing crash risk.
Winnebago is recalling 2021-2022 Inspire motorhomes because the step well cover support may be insufficient, potentially causing the step to collapse when stepped on.
USDA issued a public health alert for Trader Joe's Caesar Salad with Chicken because the dressing packets contain undeclared egg. No illnesses have been reported.
Prevost is recalling 30 units of the 2021 X3-45 commuter bus because a bolt securing the rear bench seat was not installed, creating a crash injury risk.
Mercedes-Benz is recalling 1,168 2020 GLC 350 E vehicles because a transmission wiring harness may chafe against the drive shaft, causing loss of drive power and increasing crash risk.
Isuzu is recalling 2022 FTR trucks because a missing parking pawl in the transmission could allow the vehicle to roll away, increasing crash risk.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter 2500 vehicles because an incorrectly connected generator wiring harness may cause an electrical surge, increasing the risk of a fire.
Prevost is recalling 2021-2023 X3-45 commuter buses because a seat retention pin could fail, causing the backrest to collapse and increasing injury risk in a crash.
Mercedes-Benz is recalling 8,530 vehicles because a software error may prevent the rearview camera from displaying images, increasing crash risk.