Device recall
Z-1335-2019: Tissu-Trans MEGA 1500, Catalog 3-TT-MEGA 1500, sterile, disposable, one-patient…
FDA device recall · Class II · Shippert Medical Technologies
Key facts
| Recall number (Z-number) | Z-1335-2019 |
|---|---|
| Recall event | 81837 |
| Product | Tissu-Trans MEGA 1500, Catalog 3-TT-MEGA 1500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO. |
| Product code | MUU |
| Recalling firm | Shippert Medical Technologies |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K092482 |
| FEI number | 3008719017 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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