PlainRecalls
FDA Devices Moderate Class II Ongoing

Mycoplasma test, IgG and IgM

Reported: December 10, 2025 Initiated: November 3, 2025 #Z-0746-2026

Product Description

Mycoplasma test, IgG and IgM

Reason for Recall

Distribution without premarket approval/clearance.

Details

Units Affected
23 units
Distribution
US Nationwide distribution.
Location
Vastervik

Frequently Asked Questions

What product was recalled?
Mycoplasma test, IgG and IgM. Recalled by GET TESTED INTERNATIONAL AB. Units affected: 23 units.
Why was this product recalled?
Distribution without premarket approval/clearance.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 10, 2025. Severity: Moderate. Recall number: Z-0746-2026.