FDA recall record

TEKNIMED SAS HIGH V+ Spinal Cement System REF T040321K recall — FDA Z-1099-2023

Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.

Class IIclassification
Z-1099-2023official record ID
Feb 15, 2023report date

Recall record at a glance

Official recordZ-1099-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmTEKNIMED SAS
Report dateFeb 15, 2023
Recall initiation dateDec 15, 2022
Quantity236 systems
LocationL'Union, France

Official product description

HIGH V+ Spinal Cement System REF T040321K

Why the product was recalled

Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.

Distribution information

Worldwide distribution - U.S. Nationwide distribution in the state of MS and the countries of Poland, Lithuania, Spain, Taiwan, South Africa, Israel.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.