CrossFT Punch — Class II medical device recall Z-2147-2012
Terminated recall by Linvatec Corp. dba ConMed Linvatec, reported 2012-08-15, distributed nationwide. ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT Punch because there is a possibility that the de
| Recall number | Z-2147-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec, Largo, FL, United States |
| Recall initiated | 2011-08-12 |
| Classified | 2012-08-06 |
| Reported by FDA | 2012-08-15 |
| Terminated | 2013-11-21 |
| Distributed | Nationwide (US) |
| Quantity | 2 |
| Lot numbers | 156920 |
Product
CrossFT Punch, Product Number PFT-45M. Manufacturer: CONMED LINVATEC. The intended use is to create a hole to facilitate insertion of the CrossFT suture anchor into bone.
Reason for recall
ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT Punch because there is a possibility that the device was etched incorrectly listing the item number as PFT-00M and includes incorrect depth lines for insertion.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2147-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.