Device recall
Z-1327-2011: Churchill Medical Systems LifeGuard Non-Coring Huber Needle, Lifeguard…
FDA device recall · Class II · Churchill Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1327-2011 |
|---|---|
| Recall event | 57295 |
| Product | Churchill Medical Systems LifeGuard Non-Coring Huber Needle, Lifeguard Non-Coring Safety Infusion Set 22GA, 3/4"; Item # CLG-2234 The Lifeguard |
| Product code | FPA |
| Recalling firm | Churchill Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2012 |
| 510(k) numbers | K013871 |
| 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