Device recall
Z-1796-2022: a. DERMARITE INDUSTRIES DermaCol Collagen Dressing DermaCol Without Border…
FDA device recall · Class III · Mckesson Medical-Surgical Inc. Corporate Office
Key facts
| Recall number (Z-number) | Z-1796-2022 |
|---|---|
| Recall event | 90731 |
| Product | a. DERMARITE INDUSTRIES DermaCol Collagen Dressing DermaCol Without Border Collagen / Sodium Alginate / Carboxyl Methylcellulose (CMC) / Ethylenediamine-tetraacetic Acid (EDTA) 4 X 4 Inch 10 Count Model Number: 00303E. b. DERMARITE INDUSTRIES DermaCol Ag Silver Collagen Dressing DermaCol/Ag 2 X 2… |
| Product code | FRO |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K060804 |
| FEI number | 3004386693 |
At a glance
- 1–9 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