PlainRecalls

GET TESTED INTERNATIONAL AB

63 recalls on record · Latest: Dec 10, 2025

GET TESTED INTERNATIONAL AB Recall Insight

GET TESTED INTERNATIONAL AB appears on 63 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.075% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Dec 10, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Dec 10, 2025 to Dec 10, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Small

FDA Devices Moderate Dec 10, 2025

Vitamin D-Test

FDA Devices Moderate Dec 10, 2025

Candida Test

FDA Devices Moderate Dec 10, 2025

Organic Acids Profile Test Large

FDA Devices Moderate Dec 10, 2025

Allergy Test IgE

FDA Devices Moderate Dec 10, 2025

Allergy test Small

FDA Devices Moderate Dec 10, 2025

GI Microbiome Profile XL

FDA Devices Moderate Dec 10, 2025

Illegally Marketed

FDA Devices Moderate Dec 10, 2025

HPV Antigen Test

FDA Devices Moderate Dec 10, 2025

Sperm Test

FDA Devices Moderate Dec 10, 2025

Mycoplasma test, IgG and IgM

FDA Devices Moderate Dec 10, 2025

Parasite Test

FDA Devices Moderate Dec 10, 2025

Adrenal Test

FDA Devices Moderate Dec 10, 2025

Neurotransmitters Plus

FDA Devices Moderate Dec 10, 2025

Pollen Allergy Test

FDA Devices Moderate Dec 10, 2025

Alcohol (ALC) Test Saliva

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test XL

FDA Devices Moderate Dec 10, 2025

Pet Allergy Test

FDA Devices Moderate Dec 10, 2025

Urinary Tract Infection Test

FDA Devices Moderate Dec 10, 2025

Lactose Intolerance Test

FDA Devices Moderate Dec 10, 2025

PSA Test

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Small

FDA Devices Moderate Dec 10, 2025

8 in 1 STI Test Kit

FDA Devices Moderate Dec 10, 2025

Akkermansia Test

FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Medium

FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Large

FDA Devices Moderate Dec 10, 2025

Mycotoxin Panel Test

FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Small

FDA Devices Moderate Dec 10, 2025

Allergy test Small

FDA Devices Moderate Dec 10, 2025

Peptic Ulcer Test (H, pylori)

FDA Devices Moderate Dec 10, 2025

Heavy Metals Test

FDA Devices Moderate Dec 10, 2025

Fructose Intolerance Test

FDA Devices Moderate Dec 10, 2025

Trichomonas Vaginalis test

FDA Devices Moderate Dec 10, 2025

SIBO Test

FDA Devices Moderate Dec 10, 2025

Intestinal Worms Test

FDA Devices Moderate Dec 10, 2025

D-Dimer Test

FDA Devices Moderate Dec 10, 2025

Diabetes HbA1c Test

FDA Devices Moderate Dec 10, 2025

Candida Test

FDA Devices Moderate Dec 10, 2025

Syphilis Test

FDA Devices Moderate Dec 10, 2025

Iodine Test

FDA Devices Moderate Dec 10, 2025

MPOX Test

FDA Devices Moderate Dec 10, 2025

GI Microbiome Profile Small

FDA Devices Moderate Dec 10, 2025

Parasite Test

FDA Devices Moderate Dec 10, 2025

Sperm Test

FDA Devices Moderate Dec 10, 2025

DHEA Test

FDA Devices Moderate Dec 10, 2025

Serotonin Test

FDA Devices Moderate Dec 10, 2025

Female Fertility Test

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Mega

FDA Devices Moderate Dec 10, 2025

Food Allergy Panel Test (IgE)

FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Large

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds