Device recall
Z-0346-2011: ATM100, LB-AP-M0001 Fibrijet, Catalog Number ATM100, Autoloous Thrombin Mixer…
FDA device recall · Class I · Micromedics, Inc.
Key facts
| Recall number (Z-number) | Z-0346-2011 |
|---|---|
| Recall event | 56874 |
| Product | ATM100, LB-AP-M0001 Fibrijet, Catalog Number ATM100, Autoloous Thrombin Mixer (Blending Connector), Micromedics, Sterilized by Ethylene Oxide, Rx Only, MicromedicsInc., St Paul, MN 55121-1385. Distributed by Lifebond, P.O. Box 3048 Caesarea Industrial Park 38900, Israel, LP-AP-M0001, LifeSeal SLR… |
| Product code | KYZ |
| Recalling firm | Micromedics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 21, 2011 |
| 510(k) numbers | K881020 |
| 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