Device recall
Z-0238-2012: Angiotech***Custom General Biopsy Tray for OMA North of Oklahoma City*** 1…
FDA device recall · Class II · Medical Device Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0238-2012 |
|---|---|
| Recall event | 57585 |
| Product | Angiotech***Custom General Biopsy Tray for OMA North of Oklahoma City*** 1 - 60cc Syringe; 2 - 10cc Syringe L/L; 1 -18ga x 1-1/2" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 20ga x 1-1/2" Needle; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 50cm Extension Tube; 1 - 10% Povidone Iodine Swab… |
| Product code | OJV |
| Recalling firm | Medical Device Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2011 |
| FEI number | 1036710 |
At a glance
- None Linked 510(k)s
- 10–99 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