ConvaTec DuoDERM Dressings Recall: Open Seals Risk Sterility Compromise
ConvaTec recalls DuoDERM CGF and Extra Thin Dressings due to potential open seals that could compromise sterility. Affected lots and models listed. Consumers should contact for details.
Lower-risk recall
There is a potential for open seals which can compromise sterility.
Contact the company
What happened, in plain English
ConvaTec is recalling two types of DuoDERM dressings because they might have open seals that could make them less sterile. This could lead to infections if used improperly. The recall affects specific lots and packaging. Read more at govinfonow.com/recall/62009-convatec-duoderm-dressings-recall-open-seals-risk-sterility-compromise.
Source Summary by GovInfoNow · govinfonow.com/recall/62009-convatec-duoderm-dressings-recall-open-seals-risk-sterility-compromise · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2519-2021
Cite this page
“ConvaTec DuoDERM Dressings Recall: Open Seals Risk Sterility Compromise.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62009-convatec-duoderm-dressings-recall-open-seals-risk-sterility-compromise. Based on FDA recall #Z-2519-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2519-2021%22&limit=1).
Why it’s dangerous
Open seals in the dressings could allow bacteria to enter the wound, increasing infection risk. The dressings are designed to stay sterile during use, but the seal issue might compromise that protection.
Who’s affected
Patients using these dressings for wounds or burns are most at risk. Healthcare providers and caregivers who apply the dressings may also be affected.
How to tell if you have this one
Check for the product names and lot numbers listed in the recall notice. The affected dressings include DuoDERM CGF 10x10cm (1x5PK) and DuoDERM Extra Thin 15x15cm (1x10PK) with specific lot numbers.
- Brand
ConvaTec- Category
Medical device
What to do — step by step
Check Product Lot Numbers
Look for the lot numbers listed in the recall notice to determine if your dressings are affected.
How this recall unfolded
Recall timeline
FDA published this recall 51 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
How can I tell if my dressings are affected?
Check the lot numbers listed in the recall notice: ICC 187660 (Lots 9B02984Y, 9G04308, etc.), ICC 187957 (Lots 9J02859, 9H02226, etc.), and ICC 187955 (Lots 9L01731, 9L04890, etc.).
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2519-2021 (August 9, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2519-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.