Mycoplasma test, IgG and IgM
Class I - Dangerous 🏥 Medical Devices
Recalled: November 3, 2025 GET TESTED INTERNATIONAL AB Diagnostic Equipment
Nationwide
What Should You Do?
- Check if you have this product: EAN: 7340221710030; SKU: A-MYC; UDI-DI: None; Lot/Serial Number: All Lots;
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- GET TESTED INTERNATIONAL AB
- Reason for Recall:
- Distribution without premarket approval/clearance.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Mycoplasma test, IgG and IgM
Product Codes/Lot Numbers:
EAN: 7340221710030; SKU: A-MYC; UDI-DI: None; Lot/Serial Number: All Lots;
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0746-2026
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