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.
Contamination with foreign substance matter
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.
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.
Healthcare professionals and patients using the recalled Tegaderm CHG dressings. Those with the specific UDI/DI and lot numbers are most at risk.
Check for UDI/DI numbers 10707387802223 (carton) or 30707387802227 (each) and lot number 33WWRRR on the packaging.
Look for UDI/DI numbers 10707387802223 (carton) or 30707387802227 (each) and lot number 33WWRRR on the packaging.
The recalled product is 3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R.
Check for UDI/DI numbers 10707387802223 (carton) or 30707387802227 (each) and lot number 33WWRRR on the packaging.
The recall record does not specify a remedy, so contact 3M directly for further instructions.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-0038-2025 — 3M 3M Hello, I own a 3M that is covered by recall Z-0038-2025 from 3M. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.