Device recall
Z-1094-2012: ORIGIO MIDATLANTIC DEVICES CRYOPETTE (r) Rx only Single use only CRY-PETTE-CL…
FDA device recall · Class II · ORIGIO HUMAGEN PIPETS INC.
Key facts
| Recall number (Z-number) | Z-1094-2012 |
|---|---|
| Recall event | 60824 |
| Product | ORIGIO MIDATLANTIC DEVICES CRYOPETTE (r) Rx only Single use only CRY-PETTE-CL LOT 123456 2013-10-10 Exp. date *** MADE IN THE USA STERILE R ***Origio, Inc. 3400 Hunter's Way, Charlottesville, VA 22911 www.origio.com The Cryopette (r) is a cryopreservative storage device that is intended for use in… |
| Product code | MQK |
| Recalling firm | ORIGIO HUMAGEN PIPETS INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2013 |
| 510(k) numbers | K100596 |
| FEI number | 1216677 |
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