Device recall
Z-0504-2009: Single-use sterile puncture attachment UA1256-U used with the BK Medical…
FDA device recall · Class II · Bk Medical
Key facts
| Recall number (Z-number) | Z-0504-2009 |
|---|---|
| Recall event | 50157 |
| Product | Single-use sterile puncture attachment UA1256-U used with the BK Medical Ultrasounds: Diagnostic Ultrasound scanner Pro Focus 2202 and Diagnostic Ultrasound Transducer 8667 Diagnostic Ultrasound scanner 2102 and Diagnostic Ultrasound Transducer 8667 Diagnostic Ultrasound scanner 2101 and Diagnostic… |
| Recalling firm | Bk Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2016 |
| FEI number | 3003705156 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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