Device recall
Z-1880-2011: POUCH/CARTON LABEL: ***REF 5023-138***9.5 x 25.5 x 0.4mm***QTY 1***MICRO…
FDA device recall · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-1880-2011 |
|---|---|
| Recall event | 58013 |
| Product | POUCH/CARTON LABEL: ***REF 5023-138***9.5 x 25.5 x 0.4mm***QTY 1***MICRO SAGITTAL BLADE, FINE***STERILE***Rx Only***CONMED LINVATEC, CONMED LINVATEC 11211 CONCEPT BLVD LARGO, FL 33773-4908 USA***Made in USA*** To cut soft tissue or bone |
| Product code | HWE |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2011 |
| FEI number | 1017294 |
At a glance
- None Linked 510(k)s
- 1–9 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