Device recall
Z-0358-2020: TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the…
FDA device recall · Class II · TriMed Inc.
Key facts
| Recall number (Z-number) | Z-0358-2020 |
|---|---|
| Recall event | 83820 |
| Product | TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA. |
| Product code | LXH |
| Recalling firm | TriMed Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3001236812 |
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