T-SPOT.TB REF TB.300 US
FDA Recall Z-1641-2022 · Posted None
Advertisement
Recalling FirmOXFORD IMMUNOTEC LTD
Recall StatusOpen, Classified
Product CodeOJN
Date Initiated2022-07-07
Product Quantity81 units
Reason for Recall
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.
Firm Action
On 07/07/2022, Oxford Immunotec Limited send a Field Safety Notice to customers informing them that the firm has become aware that products distributed may have been stored outside of the storage specifications for a short period. Customer are asked to quarantined the affected products until further notice.
On 07/13/2022, the firm communicated a follow-up "URGENT ACTION REQUIRED" Letter to customer asking to confirm that affected products have been segregated into a quarantine area and have not been used to produce patient results.
On 07/20/2022, the firm sent a "VOLUNTARY PRODUCT RECALL NOTIFICATION" informing customers that Oxford Immunotec Limited is conducting a full recall of the affected products and asking customers to now destroy the affected products following these steps:
1. Ensure Recalled Product remains in Quarantine. As per our previous
communication dated July-13-2022, please ensure all stock of the above
products remain in a secure location pending destruction.
2. Complete Tracking/Verification Form. Complete and return the enclosed
tracking/verification form, following the directions on this page and the
Tracking/Verification Form. Your Oxford Immunotec sales representative
can assist you in completing the form.
3. Indicate Destroyed Products on Tracking/Verification Form. The
tracking/verification form lists the [product name] and product descriptions.
Please mark the number of each type of [product] that you are destroying on
this form.
On or after 08/03/2022, Oxford Immunotec Ltd communicated an updated/follow-up customer notification with included the potential risks/harms/hazards associated with the use of the affected products.
For questions or assistance - contact Chris Dark at +44 1235 442780 or Maureen Garner at 855-NWRS-222 (855-697-7222), or alternatively any Oxford Immunotec Sales Representatives.
Root Cause
Storage
Distribution Pattern
U.S.: AL, CA, DC, GA, IN, OR, and WA O.U.S.: None
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement