OXFORD IMMUNOTEC LTD recalls AIM-V Medium REF AV.200/500

Recalled September 7, 2022 · FDA recall Z-1643-2022 · OXFORD IMMUNOTEC

Hazard

Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time. · FDA Class II

Units

6 units

Sold at

U.S.: AL, CA, DC, GA, IN, OR, and WA O.U.S.: None

Description

Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time.

Product

AIM-V Medium REF AV.200/500

Manufacturer(s)

OXFORD IMMUNOTEC LTD

Made in

United Kingdom

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →