Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0746-2026 — Mycoplasma test, IgG and IgM

U.S. FDA — Device Enforcement · Sweden · 2025-11-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0746-2026
Date of alert: 2025-11-03
Country / jurisdiction: Sweden
Risk level: Class II
Risk type: recall
Brand: GET TESTED INTERNATIONAL AB
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 7340221710030

Reported risk: Distribution without premarket approval/clearance.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0746-2026 — Mycoplasma test, IgG and IgM

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