medical MODERATE Updated 2026-06-10

DeRoyal Industries Inc recalls DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascula

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Recalled Product

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

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Hazard / Issue

Sterile wound dressing, lacks sterility assurance

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot: 63295141/UDI: None

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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