Device recall
Z-0104-2019: Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x…
FDA device recall · Class II · Valeris Medical, LLC
Key facts
| Recall number (Z-number) | Z-0104-2019 |
|---|---|
| Recall event | 80734 |
| Product | Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw, (1) #2 ForceBraid Blue, and (1) #2 ForceBraid White, 5 packages per container, Sterile, Rx. The firm name on the label is Valeris Medical, Marietta, GA. |
| Product code | MBI |
| Recalling firm | Valeris Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2020 |
| 510(k) numbers | K133036 |
| FEI number | 3010841252 |
At a glance
- 1–9 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