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Recall Observatory FDA recall evidence

Device product

Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and capturing interferon-gamma in the vicinity of these cells.

Z-2976-2020

July 16, 2020

Class III

Product summary

Firm
Oxford Immunotec
Event
Event 86003
Status
Terminated
Classification
Class III
Quantity
583 units
Official record key
device-enforcement:Z-2976-2020

Official wording

Reason: Incorrect expiration date included in test kit labeling and/or in Substrate component label.

Code information: Manufacturing Kit Lot Numbers: TEC3321847, TEC3041811.

Distribution pattern: Worldwide distribution - U.S. Nationwide distribution including in the states of AL, CO, D.C., GA, ID, IN, MD, OH, PA, TN, TX, and VA. The countries of Austria, Belgium, Czech Republic, France, Germany, Italy, Kuwait, Latvia, Netherlands, Philippines, Saudi Arabia, Singapore, South Korea, Spain, Sweden, Switzerland, Turkey, United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Incorrect expiration date included in test kit labeling and/or in Substrate component label.