3M Healthcare recalls Steri-Drape Small Towel Drapes REF 1000 due to adhesive issues causing skin injuries. Affected lots include specific UDI/DI numbers and lot codes. Consumers should stop using if skin irritation occurs.
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Additionally, 3M has observed an increase in reported adhesive related skin injuries for these affected lots.
3M Healthcare is recalling Steri-Drape Small Towel Drapes REF 1000 because the adhesive liner is hard to remove without damaging the product and has caused skin injuries. This affects medical professionals and patients using the drapes during surgery.
The adhesive layer on the drape is difficult to remove without damaging the product, which can lead to skin injuries. This issue has been reported by users, indicating a potential for irritation or injury during medical procedures.
Medical professionals and patients who use these surgical drapes during procedures are most at risk. The recall targets specific lot numbers produced between 2021 and 2023.
Check for the UDI/DI number (01)30707387057245 and lot numbers listed in the recall notice, such as 33HD8F through 33KXDH. These drapes are sold as general surgery drapes with the reference number REF 1000.
If you experience skin irritation after using the drape, stop using it immediately and contact your healthcare provider.
Check the drape's UDI/DI number (01)30707387057245 and lot numbers from the list provided in the recall notice.
3M confirmed the adhesive liner is difficult to remove without damaging the product and has caused reported skin injuries.
Look for the UDI/DI number (01)30707387057245 and lot numbers listed in the recall notice, such as 33HD8F through 33KXDH.
No, but if you experience skin irritation, stop using it and contact your healthcare provider.
We’ve drafted a message you can send 3M Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0247-2023 — 3M Healthcare 3M Healthcare Hello, I own a 3M Healthcare that is covered by recall Z-0247-2023 from 3M Healthcare. 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.