3M Tegaderm CHG Dressing Recall: Contamination Risk
3M recalls Tegaderm CHG IV securement dressings due to contamination risk. Affected units have specific UDI/DI and lot numbers. Consumers should contact 3M for details.
Lower-risk recall
Contamination with foreign substance matter
Contact the company
What happened, in plain English
3M is recalling certain Tegaderm CHG IV securement dressings because they may contain foreign substances. This could lead to contamination if used improperly. Affected units have specific UDI/DI and lot numbers. Read more at govinfonow.com/recall/54235-3m-tegaderm-chg-dressing-recall-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/54235-3m-tegaderm-chg-dressing-recall-contamination-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0038-2025
Cite this page
“3M Tegaderm CHG Dressing Recall: Contamination Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54235-3m-tegaderm-chg-dressing-recall-contamination-risk. Based on FDA recall #Z-0038-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0038-2025%22&limit=1).
Why it’s dangerous
The dressings may contain foreign substances that could contaminate the IV site. This poses a risk of infection or other complications if the dressing is used without proper cleaning.
Who’s affected
Healthcare professionals and patients using the recalled Tegaderm CHG dressings. Those with the specific UDI/DI and lot numbers are most at risk.
How to tell if you have this one
Check for UDI/DI numbers 10707387802223 (carton) or 30707387802227 (each) and lot number 33WWRRR on the packaging.
- Brand
3M- Category
Medical device
What to do — step by step
Check Product Details
Look for UDI/DI numbers 10707387802223 (carton) or 30707387802227 (each) and lot number 33WWRRR on the packaging.
How this recall unfolded
Recall timeline
FDA published this recall 2 months 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
What is the specific model of the recalled dressing?
The recalled product is 3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R.
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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-0038-2025 (August 14, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0038-2025 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.