Device recall
Z-2243-2014: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film…
FDA device recall · Class I · Cook Inc.
Key facts
| Recall number (Z-number) | Z-2243-2014 |
|---|---|
| Recall event | 68914 |
| Product | CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is supplied one pouch in a box. The CloverSnare 4-Loop Vascular Retriever is intended for use in the cardiovascular system to manipulate and retrieve foreign objects, including but not… |
| Product code | MMX |
| Recalling firm | Cook Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 16, 2015 |
| 510(k) numbers | K112185 |
| FEI number | 1820334 |
At a glance
- 1–9 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