TEKNIMED SAS Zone Industrielle Montredone 11 Rue D Apollo L'Union France HIGH V+ Spinal Cement System REF T040321K Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HIGH V+ Spinal Cement System REF T040321K
Brand
TEKNIMED SAS Zone Industrielle Montredone 11 Rue D Apollo L'Union France
Lot Codes / Batch Numbers
Model/Part Number: T040321K UDI-DI Code: 03760177043084 Batch Number: 060422382
Products Sold
Model/Part Number: T040321K UDI-DI Code: 03760177043084 Batch Number: 060422382
TEKNIMED SAS Zone Industrielle Montredone 11 Rue D Apollo L'Union France is recalling HIGH V+ Spinal Cement System REF T040321K due to Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.
Recommended Action
Per FDA guidance
On 12/15/2022, the firm contacted customer via a "URGENT - FIELD SAFETY NOTICE" informing them of the incorrect expiry date of 2027-02-28 and that the correct expiration date is 2025-02-28. Customers are instructed to: 1. Notify all within their organization or to any organizations where the devices have been transferred. 2. Isolate the concerned products in their facilities and/or in their customers' ones. 3. Complete and return by email, within 7 calendar days, the attached statement for the product return, by indicating the concerned quantity by lot and by company to TEKNIMED SAS, Quality Department quality@tekmimed.com 4. Return, all products clearly identified as recalled products and with the attached statement at the following address: Quality Department TEKNIMED SAS, Z.I. de la Herray, 65500 VIC en BIGORRE (France). For questions or assistance - contact Quality Manager at +33 5 34 25 10 60
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026