Recall Z-2305-2026— DeRoyal Industries Inc
Class II · Ongoing
Class II FDA medical device recall by DeRoyal Industries Inc, initiated 2026-05-18. FDA's recall record names no specific 510(k) clearance for this event. Product: DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm). Reason: Sterile wound dressing, lacks sterility assurance.
- Recalling firm
- DeRoyal Industries Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-05-18
- Firm location
- Powell, TN, United States
Product description
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
Reason for recall
Sterile wound dressing, lacks sterility assurance
Data sourced from openFDA. This site is unofficial and independent of the FDA.