FDA recall record

ConvaTec AQUACEL Foam Ag Adhesive, wound dressing advesive recall — FDA Z-0723-2023

ConvaTec are voluntarily recalling a batch of AQUACEL Foam Ag Adhesive 10cm x 10cm (x 10 pack) due to the identification of visual contamination in the…

Class IIclassification
Z-0723-2023official record ID
Dec 28, 2022report date

Recall record at a glance

Official recordZ-0723-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmConvaTec, Inc.
Report dateDec 28, 2022
Recall initiation dateNov 15, 2022
Quantity5300 devices
LocationGreensboro, NC, United States

Official product description

ConvaTec AQUACEL Foam Ag Adhesive, wound dressing advesive

Why the product was recalled

ConvaTec are voluntarily recalling a batch of AQUACEL Foam Ag Adhesive 10cm x 10cm (x 10 pack) due to the identification of visual contamination in the form of brown spots present on several dressings.

Distribution information

US Nationwide distribution.

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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