Device recall
Z-2252-2010: C-REAMER CANNULATED, STERILE, Rx ONLY. REF 8772A, 9.0MM, QTY DIST 712. REF…
FDA device recall · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-2252-2010 |
|---|---|
| Recall event | 54701 |
| Product | C-REAMER CANNULATED, STERILE, Rx ONLY. REF 8772A, 9.0MM, QTY DIST 712. REF 8773A, 10MM, QTY DIST 1,244. REF 8774A, 11MM, QTY DIST 384 REF 8775A, 12MM, QTY DIST 156 CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. |
| Product code | LXH |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2010 |
| FEI number | 1017294 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database