Class II

Medical Device Recall: DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)

DeRoyal Industries Inc · May 18, 2026

Reason for Recall

Sterile wound dressing, lacks sterility assurance

Distribution

US Nationwide distribution in the states of FL & NC.

States Affected

NATIONWIDE

Quantity Affected

800 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2305-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.