Get Tested International Ab

Complete recall history across all FDA and CPSC categories — 92 total recalls

Get Tested International Ab appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (92)

FDA medical device enforcement actions by Get Tested International Ab. Showing most recent 50.

Date Product Reason Class
Nov 3, 2025 Continuous Glucose Monitor (CGM) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Estrogen & Progesterone Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Gut Microbiome Test Medium Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Vaginal PH Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Environmental Pollutants Profile Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Sorbitol Intolerance Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 IBS Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Neurotransmitters XL Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Melatonin Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Women s Hormone Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Fecal Occult Blood Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Epstein-Barr Virus (EBV VCA & EBNA IgG) Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Neurotransmitters Basic Distribution without premarket approval/clearance. Class II
Nov 3, 2025 H pylori (Peptic ulcer) Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Men s Hormone Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Food Sensitivity Test Medium Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Ovulation Test (5 tests) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Allergy & Food Intolerance Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Pregnancy Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Liver Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Diabetes Test (ketones & glucose) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Iron Deficiency Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Herpes (HSV-1 & HSV-2) Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Thyroid TSH Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Iron Deficiency Test (ferritin) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Cholesterol Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Gonorrhea test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Chlamydia Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Gut Microbiome Test Large Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Hair Mineral Analysis Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Organic acids Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Drug Test Small (4 substances) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Lyme Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Biological Age & Longevity Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 3 in 1 STI Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Blood Type Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Menopause (FSH) 2 Tests Distribution without premarket approval/clearance. Class II
Nov 3, 2025 2 in 1 Trichomonas / Gardnerella Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Kidney Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Leaky Gut Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Vitamin D2 and D3 Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 NAD Profile Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Food Intolerance Test Large Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Food Allergy Panel Test (IgE) Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Gut Microbiome Test Mega Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Female Fertility Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Serotonin Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 DHEA Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Sperm Test Distribution without premarket approval/clearance. Class II
Nov 3, 2025 Parasite Test Distribution without premarket approval/clearance. Class II

View all 92 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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