"***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*
FDA device recall Z-0164-2013 · posted 2012-10-29 · Terminated
Recall details
- Recalling firm
- Linvatec Corp. dba ConMed Linvatec
- Reason for recall
- ConMed Linvatec is recalling the product due to the punch being mis-assembled with the incorrect handled. The correct handle is a clear anodized silver colored handle.
- Action taken
- Linvatec Corp sent a Urgent Medical Device Recall Notification letter dated April 9, 2012, to all affected customers. The letter was sent via FEDEx and by e-mail. The letter identified the product the problem and the action needed to be taken by the customer. Customers were instructed to check their inventory for the recalled product and segregate them for return to the recalling firm. Furthermore, return the products along with the "REPLY FORM". Should you have any further questions please contact our Customer Service department at (800) 237-0169.
- Root cause
- Process control
- Status
- Terminated
- Product code
- LXH
- Quantity affected
- 2 units
- Distribution
- Worldwide Distribution--US (nationwide) including state of Minnesota and the country of Thailand
- Date initiated
- 2012-04-09
- Date posted
- 2012-10-29
- Date terminated
- 2013-11-21
- Location
- Largo, FL
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