Device recall
Z-1502-2021: Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921…
FDA device recall · Class II · Medela AG Medical Technology
Key facts
| Recall number (Z-number) | Z-1502-2021 |
|---|---|
| Recall event | 87551 |
| Product | Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump. |
| Product code | BTA |
| Recalling firm | Medela AG Medical Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2024 |
| 510(k) numbers | K170329 |
| FEI number | 3002807523 |
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