Device recall
Z-0410-2018: TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE
FDA device recall · Class II · Somatex Medical Technologies GmbH
Key facts
| Recall number (Z-number) | Z-0410-2018 |
|---|---|
| Recall event | 78349 |
| Product | TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE |
| Product code | NEU |
| Recalling firm | Somatex Medical Technologies GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2018 |
| 510(k) numbers | K073095 |
| FEI number | 1000408433 |
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