Device recall
Z-0345-2011: AMS600-B, AMS700-B, SA-0105, SA-3675, SA-3678 Arteriocyte Medical systems…
FDA device recall · Class I · Micromedics, Inc.
Key facts
| Recall number (Z-number) | Z-0345-2011 |
|---|---|
| Recall event | 56874 |
| Product | AMS600-B, AMS700-B, SA-0105, SA-3675, SA-3678 Arteriocyte Medical systems, Magellan, Cannula Tip, Catalog Number AMS600-B,Sterilized by Ethylene Oxide, Rx Only, Manufacturer Micromedics Inc., St. Paul, MN 55121-1385 USA, Distributor: Arteriocyte Medical Systems, Inc., 45 South Street, Hopkinton, MA… |
| Product code | KYZ |
| Recalling firm | Micromedics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 21, 2011 |
| 510(k) numbers | K883338 |
| FEI number | 2183425 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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