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 the Lactose Intolerance Test due to distribution without FDA premarket clearance. The product was distributed nationwide without required regulatory approval.
GET TESTED INTERNATIONAL AB distributed the Gut Microbiome Test Small nationwide without FDA premarket approval or clearance. Consumers should stop using the product.
GET TESTED INTERNATIONAL AB is recalling Vitamin D-Test devices distributed without FDA premarket approval or clearance. The unapproved medical devices have not undergone FDA safety and efficacy review.
GET TESTED INTERNATIONAL AB is recalling the DHEA Test (all lots) that was distributed nationwide in the US without required FDA premarket approval or clearance.
Food Intolerance Test Medium was distributed nationwide without FDA premarket approval or clearance. The product requires regulatory review before being sold in the United States.
GET TESTED INTERNATIONAL AB is recalling the Mycotoxin Panel Test because it was distributed without FDA premarket approval. Consumers should stop using the product.
GET TESTED INTERNATIONAL AB is recalling Iodine Test units distributed nationwide due to distribution without FDA premarket approval or clearance. No illnesses or injuries have been reported.
GET TESTED INTERNATIONAL AB recalled its 8 in 1 STI Test Kit after distributing 2043 units nationwide without FDA premarket approval or clearance. The unapproved device poses a risk of unreliable or inaccurate test results.
GET TESTED INTERNATIONAL AB distributed the Heavy Metals Test nationwide without FDA premarket clearance. The company is recalling all 50 units across all lots.
GET TESTED INTERNATIONAL AB is recalling the Intestinal Worms Test (all lots) distributed nationwide without FDA premarket approval. The device has not undergone required regulatory review.
GET TESTED INTERNATIONAL AB recalled all 60 units of its Trichomonas Vaginalis diagnostic test distributed nationwide in the US without FDA premarket approval or clearance.
Akkermansia Test, manufactured by GET TESTED INTERNATIONAL AB, was distributed nationwide without required FDA premarket approval. All lot numbers are affected.
GET TESTED INTERNATIONAL AB is recalling its MPOX Test nationwide due to distribution without FDA premarket approval or clearance. Consumers who have purchased this test should not use it.
GET TESTED INTERNATIONAL AB is recalling GI Microbiome Profile XL for distribution without FDA premarket approval or clearance. All lots were distributed nationwide in the United States.
GET TESTED INTERNATIONAL AB is recalling Hair Mineral Analysis kits distributed nationwide without FDA premarket approval. Consumers should stop using this product.
GET TESTED INTERNATIONAL AB is recalling its HPV Antigen Test (258 units, all lots) nationwide due to distribution without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB distributed a medical device without FDA premarket approval or clearance. The device was distributed nationwide in the United States.
Adrenal Test kits distributed nationwide by GET TESTED INTERNATIONAL AB are being recalled because they were distributed without FDA premarket approval or clearance. Users should discontinue use immediately.
GET TESTED INTERNATIONAL AB recalled 27 units of the PSA Test distributed nationwide without FDA premarket approval or clearance.
Food Sensitivity Test Small kits are recalled for distribution without FDA premarket approval or clearance. Consumers should stop using and contact the manufacturer.
GET TESTED INTERNATIONAL AB is recalling its Fructose Intolerance Test because the product was distributed in the United States without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling Syphilis Test kits (528 units, all lots) that were distributed nationwide without FDA approval or clearance. The device was marketed without required regulatory authorization.
The FDA has recalled the Gut Microbiome Test Mega, a medical device manufactured by GET TESTED INTERNATIONAL AB, for distribution without premarket approval or clearance. The product was distributed nationwide.
GET TESTED INTERNATIONAL AB recalls its Vitamin D2 and D3 Test (EAN: 7340221709232) distributed nationwide without FDA premarket approval. All lots are affected.
A drug test device (4 substances) manufactured by GET TESTED INTERNATIONAL AB was distributed nationwide without FDA premarket clearance. Consumers should discontinue use and consult a healthcare provider.