Wound Dressing Recall: DeRoyal Covaderm Plus
Announced 2026-06-10 · FDA
The recall involves Covaderm Plus vascular access dressing (6"x6"), a sterile wound dressing, due to lack of sterility assurance. About 800 units have been distributed nationwide in Florida and North Carolina. The recall lot is 63295141 and UDI is None.
| Brand | DeRoyal Industries Inc |
|---|---|
| Product | DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm) |
| Reason | Sterile wound dressing, lacks sterility assurance |
| Severity | moderate |
| Units affected | 800 |
| Distribution | US Nationwide distribution in the states of FL & NC. |
| Agency | FDA |
| Recall / campaign no. | Lot: 63295141/UDI: None |
WHAT YOU SHOULD DO
- Do not use dressings from lot 63295141.
- Contact DeRoyal or your supplier for return or disposal instructions.
- If you experience any adverse effects, consult a healthcare professional.
- Keep the packaging and recall information for reference.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.