Device recall
Z-2340-2017: ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series…
FDA device recall · Class I · Oscor, Inc.
Key facts
| Recall number (Z-number) | Z-2340-2017 |
|---|---|
| Recall event | 76884 |
| Product | ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series. Model codes: 53912 - MDTS ATAR REUSABLE, 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE, ATAR-A DARK BLUE REUSABLE, ATAR-MDT REUSABLE, ATAR-MDT2 REUSABLE, ATAR-MDT2S-A… |
| Product code | IKD |
| Recalling firm | Oscor, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 15, 2024 |
| 510(k) numbers | K070926 |
| FEI number | 1035166 |
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