Deroyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
DeRoyal Industries is recalling Covaderm Plus Vascular Access Dressing (6"x6") because the sterile wound dressing does not meet sterility requirements. The product was distributed nationwide, with primary distribution in Florida and North Carolina. This is a Class II recall, meaning the dressing may not be safe to use as a sterile medical device.
- Recalling firm
- 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
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-05-18
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of FL & NC.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/4fbbf46e-2868-4286-897b-aaf797675f25