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
Sedecal is recalling 14 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling six SM-40HF-B-D-C 40KW.002 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM_40HF_BDC3 mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling 22 uCT 550 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
CPM Medical Consultants is updating the Fuse ULTRA Foot Plating System instructions for use to remove a sterilization option that does not apply in the United States.
Sedecal is recalling nine SM-40HF-Batt 40KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW 55C/60C mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.
Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system, serial G41234, after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 24 RadPro Mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling eight SM-32HF-B-D-C 32KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling eight uCT 530 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg across several lots after routine stability testing returned an out-of-specification result for highest unknown impurity.
Sedecal is recalling six SM-40HF-B-D-C 40KW Canon Ready mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg in 10-capsule blister packs after routine stability testing returned an out-of-specification result for highest unknown impurity.
UIH Technologies is recalling 95 uMI 550 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.
Sedecal is recalling one SM-20HF-Batt 20KW analog mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
ibspot is recalling three boxes of Taoscare Motion Sickness Patches because the product was marketed without an approved new drug application.
Sedecal is recalling eight model 40KWFXPLUS.002 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 56 SM-40HF-B-D-KM (AeroDR X30) mobile digital diagnostic X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 181 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
JB Chemicals is recalling 9,936 hundred-count bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.
UIH Technologies is recalling three uMI 780 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.
Sedecal is recalling one 40KW-FX.899 mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.