Device recall
Z-2080-2012: Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm…
FDA device recall · Class II · Beekley Corporation
Key facts
| Recall number (Z-number) | Z-2080-2012 |
|---|---|
| Recall event | 62432 |
| Product | Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plate. |
| Product code | IZH |
| Recalling firm | Beekley Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 9, 2013 |
| 510(k) numbers | K073262 |
| FEI number | 3000204334 |
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