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 |
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.
How to identify the recalled item
| Lot / date codes | Lot: 63295141/UDI: None |
|---|---|
| Lot / date codes | Lot: 63295141/UDI: None |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
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.