Device recall
Z-0154-2008: Precept Medical Products, Foam Fog Shield Surgical Mask Green Fiberglass Free…
FDA device recall · Class II · Precept Medical Products, Inc.
Key facts
| Recall number (Z-number) | Z-0154-2008 |
|---|---|
| Recall event | 45435 |
| Product | Precept Medical Products, Foam Fog Shield Surgical Mask Green Fiberglass Free, REORDER #: 65-3320, non-sterile, 25/box, 6 box/case, Precept Medical Products, Inc., Arden, NC 28704, 1-800-438-5827, Mexico |
| Product code | FYA |
| Recalling firm | Precept Medical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2009 |
| FEI number | 1018223 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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