Manufacturer
92 recalls in our database name GET TESTED INTERNATIONAL AB as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
GET TESTED INTERNATIONAL AB is recalling its Diabetes Test kit (ketones & glucose) because it was distributed nationwide without FDA premarket approval. Consumers should discontinue use and consult their healthcare provider.
GET TESTED INTERNATIONAL AB is recalling its Allergy & Food Intolerance Test (all lots) because it was distributed nationwide without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling Ovulation Test (5 tests) nationwide due to distribution without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling the Sorbitol Intolerance Test distributed nationwide because it was sold without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling Gut Microbiome Test Medium nationwide because the product was distributed without FDA premarket approval. Consumers should discontinue use.
GET TESTED INTERNATIONAL AB is recalling Gut Microbiome Test XL nationwide because the device was distributed without FDA premarket approval or clearance. Consumers should discontinue use and contact the manufacturer.
GET TESTED INTERNATIONAL AB is recalling its Pet Allergy Test product (EAN: 616612785695) distributed in the U.S. without FDA premarket approval or clearance. Approximately 29 units distributed nationwide are subject to this Class II recall.
GET TESTED INTERNATIONAL AB is recalling Peptic Ulcer Test (H. pylori) due to distribution without FDA premarket approval or clearance. Consumers should discontinue use and consult their healthcare provider.
GET TESTED INTERNATIONAL AB is recalling the NAD Profile Test (all lots) because it was distributed without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB's Sperm Test (EAN 7340221710221, all lots) was distributed nationwide without required FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling 658 units of Parasite Test distributed nationwide without FDA premarket approval. The device lacks FDA validation for safety and effectiveness.
GET TESTED INTERNATIONAL AB is recalling its Serotonin Test distributed nationwide because the device was marketed without required FDA premarket approval or clearance. Stop using the product and contact the manufacturer for return instructions.
GET TESTED INTERNATIONAL AB is recalling the Female Fertility Test nationwide. The product was distributed without FDA premarket approval or clearance, which is required for medical devices.
GET TESTED INTERNATIONAL AB is recalling the Food Intolerance Test Large (EAN: 616612785640) that was distributed nationwide without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling 754 units of its 2 in 1 Trichomonas / Gardnerella Test that was distributed nationwide without FDA premarket approval or clearance. The recall affects all lots.
GET TESTED INTERNATIONAL AB is recalling an Iron Deficiency Test (ferritin) that was distributed without FDA premarket approval. All lots should not be used.
Food Sensitivity Test Medium manufactured by GET TESTED INTERNATIONAL AB has been recalled due to distribution without FDA premarket approval. Consumers should stop using and dispose of the product.