PlainRecalls
FDA Devices Moderate Class II Ongoing

Preview Strep A, Streptococcal A rapid test kits, Part Numbers: a) PRE-STA-25, b) PRE-STA-A-10

Reported: June 19, 2024 Initiated: April 22, 2024 #Z-2030-2024

Product Description

Preview Strep A, Streptococcal A rapid test kits, Part Numbers: a) PRE-STA-25, b) PRE-STA-A-10

Reason for Recall

Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or direct-to-consumer customers.

Details

Recalling Firm
Wondfo USA Co Ltd
Units Affected
1,238,755 units
Distribution
US Nationwide distribution.
Location
Willowbrook, IL

Frequently Asked Questions

What product was recalled?
Preview Strep A, Streptococcal A rapid test kits, Part Numbers: a) PRE-STA-25, b) PRE-STA-A-10. Recalled by Wondfo USA Co Ltd. Units affected: 1,238,755 units.
Why was this product recalled?
Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or direct-to-consumer customers.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 19, 2024. Severity: Moderate. Recall number: Z-2030-2024.