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FDA Medical Device Recalls (openFDA)

Oxford Immunotec: 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.

Recall number
Z-2976-2020
Recalling firm
Oxford Immunotec
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.
Status
Terminated
Initiated
2020-07-16
Posted
not on file
Terminated
2021-09-13
Reason
Incorrect expiration date included in test kit labeling and/or in Substrate component label.
Root cause
Labeling False and Misleading
Action
The recall letters were sent to consignees on July 16, 2020 and sent via certified mail (return receipt). Actions to be taken by the Customer/User: Locate the product in possession, and any in central supply departments, and note the quantity remaining on the verification form attached to this notification. Return the completed form following the instructions below. Then collection of the remaining product will be arranged and shipment of the replacement product. If there has been further distribution of the affected lot number also forward the notification to the appropriate end users. NOTE: NO OTHER LOTS OR PRODUCTS ARE INVOLVED IN THIS RECALL.. There is an enclosed verification form to acknowledge that the recall notice has been received and to document the quantity remaining in stock for return and replacement. Complete the form immediately indicating one of the following options: - There is no remaining stock of the aforementioned kit lots. - There is stock of the aforementioned kit lots remaining in inventory. Record the quantity of stock remaining for replacement. The verification form should be sent via email to Ben Hamilton at bhamilton@oxfordimmunotec.com, even if there is no product remaining in inventory. The completed form should also be returned using a prepaid enclosed envelope . Upon receipt of the completed and returned verification form, there will be contact to arrange courier collection of any remaining stock, and be provided information as to when replacement stock will be shipped. Other Information: For questions regarding this voluntary recall notification, or would like assistance with this recall, call: - Ben Hamilton at +44 1235 442619, Monday through Friday, 8 am to 12 pm Eastern Time - Alternatively, call the toll-free number at 1-877-208-7768, Monday through Friday, 8 am to 12 pm Eastern Time. Following the automated instructions, dial 4 to go through to the name directory and request Ben Hamilton. If no one is available t
Quantity
583 units
Distribution
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.
Lot, serial or model codes
Manufacturing Kit Lot Numbers: TEC3321847, TEC3041811.
510(k) numbers
not on file
PMA numbers
not on file
Product code
OJN
Firm FEI
3006017427
Firm city
Abingdon
Firm state
not on file
Firm country
United Kingdom

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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