XTANT Medical Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
Brand
XTANT Medical
Lot Codes / Batch Numbers
LOT: XS1920458A
Products Sold
LOT: XS1920458A
XTANT Medical is recalling Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591 due to The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
Recommended Action
Per FDA guidance
On May 12, 2020 a customer letter (in an envelope marked URGENT) was Federal Expressed priority overnight-signature required to the three customers who received the affected devices. On May 19, 2020, an additional customer letter (in an envelope marked URGENT) was Federal Expressed priority overnight-signature required to one of the three affected customers.
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 noticeDistribution
As reported by FDA
AZ, TX, WV
Page updated: Jan 10, 2026