Device recall
Z-2703-2011: "***LINVATEC SRS SHOULDER RESTORATION SYSTEM CrossFT 5.5mm CrossFT Suture Anchor…
FDA device recall · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-2703-2011 |
|---|---|
| Recall event | 58936 |
| Product | "***LINVATEC SRS SHOULDER RESTORATION SYSTEM CrossFT 5.5mm CrossFT Suture Anchor with Two#2 (5 metric) Hi-Fi Sutures***SRS.Linvatec.com***ConMed Linvatec Biomaterials, Ltd. Hemiankatu 6-8L 33720 Tampere, FINLAND***STERILE EO***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA Made in… |
| Product code | MBI |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 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