Device recall
Z-1326-2011: Churchill Medical Systems 6" Microbore Trifurcated non-DEHP Extension Set with…
FDA device recall · Class II · Churchill Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1326-2011 |
|---|---|
| Recall event | 57295 |
| Product | Churchill Medical Systems 6" Microbore Trifurcated non-DEHP Extension Set with male/Female Luer Locks Slide Clamps & 0.2 Micron Filter Item Number: AMS-944 Intended use: Intravascular Administration Set |
| Product code | FPA |
| Recalling firm | Churchill Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2012 |
| 510(k) numbers | K021395 |
| FEI number | 1000120555 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 1,000+ 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