Device recall
Z-0170-2015: Rapid Neg BP Combo Panel Type 3; Catalog number B 1017-117. MicroScan Rapid…
FDA device recall · Class I · Siemens Healthcare Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-0170-2015 |
|---|---|
| Recall event | 69540 |
| Product | Rapid Neg BP Combo Panel Type 3; Catalog number B 1017-117. MicroScan Rapid panels are designed for use in determining identification to the species level and/or antimicrobial agent susceptibility of rapidly growing aerobic and facultatively anaerobic gram negative bacilli. |
| Product code | LON |
| Recalling firm | Siemens Healthcare Diagnostics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 29, 2015 |
| PMA numbers | P870049 |
| FEI number | 2919016 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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