3M Steri-DrapeRecalls & reported problems across all models
3m Company · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one 3M Steri-Drape model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 4
We found 4 models of 3M Steri-Drape by 3m Company in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
4 FDA recall records name at least one of these models by its device identifier, 4 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
3M Steri-Drape recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Oct 6, 2022Open, Classified
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.
Z-0263-2023 · Root cause: Component change control · Recall details · FDA record ↗
- Oct 6, 2022Open, Classified
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.
Z-0261-2023 · Root cause: Component change control · Recall details · FDA record ↗
- Oct 6, 2022Open, Classified
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.
Z-0258-2023 · Root cause: Component change control · Recall details · FDA record ↗
- Oct 6, 2022Open, Classified
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.
Z-0256-2023 · Root cause: Component change control · Recall details · FDA record ↗
3M Steri-Drape models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- 3M™ Steri-Drape™ 1030NSDrape, surgical, exempt1 recall0 reports
- 3M™ Steri-Drape™ 1060NSDrape, surgical, exempt1 recall0 reports
- 3M™ Steri-Drape™ 1061NSDrape, surgical, exempt1 recall0 reports
- 3M™ Steri-Drape™ 1022NSDrape, surgical, exempt1 recall0 reports
Other 3m Company products
- Steri-Drape11 models · 7 reports · 8 recalls
- 3M Attest5 models · 1 reports · 4 recalls
- Ranger10 models · 176 reports
- 3M Ranger3 models · 73 reports · 1 recall
- Attest2 models · 0 reports · 2 recalls
- 3M Red Dot8 models · 16 reports · 1 recall
- Fast Release Varnish2 models · 2 reports · 1 recall
- Comply3 models · 1 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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