Device recall
Z-2072-2023: SurgiMend 2.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes…
FDA device recall · Class II · TEI Biosciences, Inc.
Key facts
| Recall number (Z-number) | Z-2072-2023 |
|---|---|
| Recall event | 92481 |
| Product | SurgiMend 2.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x20 cm, 20x25cm, 10x15cm Semi-Oval, |
| Product code | FTM |
| Recalling firm | TEI Biosciences, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K083898 |
| FEI number | 3004170064 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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