PlainRecalls

Get Tested International Ab

Compiled from official public sources by the editorial team.

92 recalls on record · Latest: Dec 10, 2025

Get Tested International Ab Recall Insight

Get Tested International Ab appears on 92 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.090% 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 42 entries, severity tagging shows 0 critical, 42 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 42 of 42 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 (42). 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

NAD Profile Test

FDA Devices Moderate Dec 10, 2025

Vitamin D2 and D3 Test

FDA Devices Moderate Dec 10, 2025

Leaky Gut Test

FDA Devices Moderate Dec 10, 2025

Kidney Test

FDA Devices Moderate Dec 10, 2025

2 in 1 Trichomonas / Gardnerella Test

FDA Devices Moderate Dec 10, 2025

Menopause (FSH) 2 Tests

FDA Devices Moderate Dec 10, 2025

Blood Type Test

FDA Devices Moderate Dec 10, 2025

3 in 1 STI Test

FDA Devices Moderate Dec 10, 2025

Biological Age & Longevity Test

FDA Devices Moderate Dec 10, 2025

Lyme Test

FDA Devices Moderate Dec 10, 2025

Drug Test Small (4 substances)

FDA Devices Moderate Dec 10, 2025

Organic acids Test

FDA Devices Moderate Dec 10, 2025

Hair Mineral Analysis

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Large

FDA Devices Moderate Dec 10, 2025

Chlamydia Test

FDA Devices Moderate Dec 10, 2025

Gonorrhea test

FDA Devices Moderate Dec 10, 2025

Cholesterol Test

FDA Devices Moderate Dec 10, 2025

Iron Deficiency Test (ferritin)

FDA Devices Moderate Dec 10, 2025

Thyroid TSH Test

FDA Devices Moderate Dec 10, 2025

Herpes (HSV-1 & HSV-2) Test

FDA Devices Moderate Dec 10, 2025

Iron Deficiency Test

FDA Devices Moderate Dec 10, 2025

Diabetes Test (ketones & glucose)

FDA Devices Moderate Dec 10, 2025

Liver Test

FDA Devices Moderate Dec 10, 2025

Pregnancy Test

FDA Devices Moderate Dec 10, 2025

Allergy & Food Intolerance Test

FDA Devices Moderate Dec 10, 2025

Ovulation Test (5 tests)

FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Medium

FDA Devices Moderate Dec 10, 2025

Men s Hormone Test

FDA Devices Moderate Dec 10, 2025

H pylori (Peptic ulcer) Test

FDA Devices Moderate Dec 10, 2025

Neurotransmitters Basic

FDA Devices Moderate Dec 10, 2025

Epstein-Barr Virus (EBV VCA & EBNA IgG) Test

FDA Devices Moderate Dec 10, 2025

Fecal Occult Blood Test

FDA Devices Moderate Dec 10, 2025

Women s Hormone Test

FDA Devices Moderate Dec 10, 2025

Melatonin Test

FDA Devices Moderate Dec 10, 2025

Neurotransmitters XL

FDA Devices Moderate Dec 10, 2025

IBS Test

FDA Devices Moderate Dec 10, 2025

Sorbitol Intolerance Test

FDA Devices Moderate Dec 10, 2025

Environmental Pollutants Profile Test

FDA Devices Moderate Dec 10, 2025

Vaginal PH Test

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Medium

FDA Devices Moderate Dec 10, 2025

Estrogen & Progesterone Test

FDA Devices Moderate Dec 10, 2025

Continuous Glucose Monitor (CGM)

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Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.