Device recall
Z-0973-03: Resolve Systems Cerebrospinal Fluid Test Kit, 50 tests per kit, Catalog…
FDA device recall · Class II · PerkinElmer LIfe Sciences Inc
Key facts
| Recall number (Z-number) | Z-0973-03 |
|---|---|
| Recall event | 26227 |
| Product | Resolve Systems Cerebrospinal Fluid Test Kit, 50 tests per kit, Catalog #FR-8050. |
| Recalling firm | PerkinElmer LIfe Sciences Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 24, 2008 |
| 510(k) numbers | K843122 |
| FEI number | 1522510 |
At a glance
- 1–9 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