Device recall
Z-0894-2011: Blood Center Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use…
FDA device recall · Class II · Continental Medical Labs,Inc
Key facts
| Recall number (Z-number) | Z-0894-2011 |
|---|---|
| Recall event | 57463 |
| Product | Blood Center Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use, Reorder No. Q921CL, Manufactured for : Blood Center of Wisconsin, Milwaukee, WI. Port VAD Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use, Reorder No. 3540CL, Manufactured for : McCormick Medical… |
| Product code | OFM |
| Recalling firm | Continental Medical Labs,Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 5, 2012 |
| FEI number | 2128604 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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