Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
J Deluca Fish Company is recalling approximately 69,590 pounds of frozen Yellow Walking Fish imported from Vietnam without required import inspection.
Golden State Medical Supply is recalling Losartan Potassium Tablets because FDA labs found an impurity above acceptable levels.
Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because FDA labs confirmed an impurity above acceptable levels.
Ortho-Clinical Diagnostics is recalling VITROS XT 7600 Integrated Systems because sample fluid may be dispensed to incorrect positions, potentially causing erroneous assay results.
DESHI DISTRIBUTORS, LLC is recalling Deshi Golden Raisins due to elevated levels of undeclared sulfites found by NYS.
Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.
Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.
Richwell Group is recalling 160,020 pounds of frozen fish products imported from Vietnam without proper inspection. No illnesses have been reported.
Blue Bird is recalling certain 2015-2020 Vision and All American non-school buses because driver-side rear brakes may drag, posing a fire and injury risk.
Blue Bird is recalling 2015-2020 Vision and All American school buses because the driver-side rear brakes may drag, posing a fire and injury risk.
Keystone is recalling 2019-2020 Dutchmen Voltage 4185 trailers because an undersized fifth wheel pin box may fail under heavy loads, increasing crash risk.
Forest River is recalling 2018-2019 Starcraft All Star XL diesel vehicles because the fuel heater may overheat, melt plastic, and cause a fire or engine stall.
Sikorski Sausages Co., Ltd. is recalling approximately 74 pounds of imported meat and poultry sausages that were not presented for import re-inspection into the United States.
Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may appear closed but are unlatched, increasing crash risk.
Meritor is recalling specific steer axles because insufficient lubrication may damage wheel end bearings, potentially causing wheel separation and loss of vehicle control.
Keystone RV Company is recalling 2018-2020 Fuzion 429 recreational trailers because a pinched wiring harness may short circuit and cause a fire.
Transfer Flow is recalling rear brake lines for mobility van conversions due to incorrect tube nut fittings that may cause a pressure drop in the braking system.
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.
Aurora Packing Company is recalling approximately 62,112 pounds of raw beef products that may be contaminated with E. coli O157:H7. The products were shipped nationwide for further distribution and processing.
AmeriHerb International Inc is recalling 1 lb bags of dried dill weed potentially contaminated with E. coli. The product was distributed nationwide and to Canada.
Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.
Jensen Tuna Inc is recalling frozen ground tuna packages due to a potential contamination with Salmonella. The product was distributed to multiple states.
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers because they may have an insufficient firing stroke to break the washer and completely form staples.