Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

AIM-V Medium REF AV.200/500 Recalled by OXFORD IMMUNOTEC LTD Due to Due to equipment failure, affected products were stored...

Date: July 7, 2022
Company: OXFORD IMMUNOTEC LTD
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact OXFORD IMMUNOTEC LTD directly.

Affected Products

AIM-V Medium REF AV.200/500

Quantity: 6 units

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 7 states: AL, CA, GA, IN, OR, WA, DC

Affected (7 states)Not affected

About OXFORD IMMUNOTEC LTD

OXFORD IMMUNOTEC LTD has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report