Device recall
Z-0951-04: 100 Sheer Plastic Spot Bandages, 7/8" Dia. (22 mm). Reorder No. 3607…
FDA device recall · Class II · Dynarex Corporation
Key facts
| Recall number (Z-number) | Z-0951-04 |
|---|---|
| Recall event | 29031 |
| Product | 100 Sheer Plastic Spot Bandages, 7/8" Dia. (22 mm). Reorder No. 3607. Manufactured for dynarex Corporation, Orangeburg, NY 10962. Sterile with non-stick pad. 100% Latex Free Bandage & Wrapper. 48 boxes of 100 bandages per case. --- Device Listing # E177598. 510(k) Exempt. |
| Product code | FQM |
| Recalling firm | Dynarex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2012 |
| FEI number | 2431014 |
At a glance
- None 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