FDA recall record

ConvaTec DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings recall — FDA Z-0160-2026

Wound dressing may have foreign matter on the product.

Class IIclassification
Z-0160-2026official record ID
Oct 22, 2025report date

Recall record at a glance

Official recordZ-0160-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmConvaTec, Inc.
Report dateOct 22, 2025
Recall initiation dateAug 29, 2025
Quantity80,980
LocationGreensboro, NC, United States

Official product description

DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly exudating wounds. DuoDERM" Extra Thin dressings are particularly suitable in areas subject to friction and those requiring contouring, e.g., elbows, heels. DuoDERM" Extra Thin dressings interact with wound moisture producing a soft mass that enables removal of the dressing with little or no damage to newly formed tissues. They help isolate the wound against bacterial and other external contamination. INDICATIONS " Management of superficial, dry to lightly exudating dermal ulcers. " Post-operative wounds. " Protective dressings.

Why the product was recalled

Wound dressing may have foreign matter on the product.

Distribution information

US Nationwide distribution including in the states of OH, AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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