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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Vaginal PH Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Urinary Tract Infection Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Trichomonas Vaginalis test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Thyroid TSH Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Syphilis Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Sperm Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Pregnancy Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Parasite Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Ovulation Test (5 tests)
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Mycoplasma test, IgG and IgM
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls MPOX Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Menopause (FSH) 2 Tests
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Lyme Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Iron Deficiency Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls HPV Antigen Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Herpes (HSV-1 & HSV-2) Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls H pylori (Peptic ulcer) Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Gonorrhea test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Female Fertility Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Fecal Occult Blood Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Epstein-Barr Virus (EBV VCA & EBNA IgG) Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Drug Test Small (4 substances)
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Illegally Marketed
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Diabetes HbA1c Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls D-Dimer Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Chlamydia Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Candida Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Blood Type Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls Alcohol (ALC) Test Saliva
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
Medtronic, Inc. recalls Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product
Hazard: There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.