Home / Brands / OXFORD IMMUNOTEC
OXFORD IMMUNOTEC Recalls
5 recalls on record · September 23, 2020 to September 7, 2022 · Medical Devices
Recalls by year
20
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 7, 2022Medical DevicesFDA
OXFORD IMMUNOTEC LTD recalls AIM-V Medium REF AV.200/500
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.
September 7, 2022Medical DevicesFDA
OXFORD IMMUNOTEC LTD recalls T-Cell Xtend REF TTK.610 US
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.
September 7, 2022Medical DevicesFDA
OXFORD IMMUNOTEC LTD recalls T-SPOT.TB REF TB.300 US
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.
September 23, 2020Medical DevicesFDA
Oxford Immunotec recalls Model No:T-SPOT.TB50, Catalogue No.: TB.50; UDI: 1505171600004 - Product Usage: intended for use as an aid in the diagno
Hazard: Incorrect expiration date included in test kit labeling and/or in Substrate component label.
September 23, 2020Medical DevicesFDA
Oxford Immunotec recalls Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the diagno
Hazard: Incorrect expiration date included in test kit labeling and/or in Substrate component label.