PlainRecalls
FDA Devices Moderate Class II Ongoing

Vitamin D2 and D3 Test

Reported: December 10, 2025 Initiated: November 3, 2025 #Z-0768-2026

Product Description

Vitamin D2 and D3 Test

Reason for Recall

Distribution without premarket approval/clearance.

Details

Units Affected
10 units
Distribution
US Nationwide distribution.
Location
Vastervik

Frequently Asked Questions

What product was recalled?
Vitamin D2 and D3 Test. Recalled by GET TESTED INTERNATIONAL AB. Units affected: 10 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-0768-2026.