# FDA recall Z-0262-2023

> **3M Healthcare Business** · Class II · device recall initiated 2022-10-06.

## Product

3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061, general surgery drape

## Reason for recall

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.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0262-2023
- **Recalling firm:** 3M Healthcare Business
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-06
- **Report date:** 2022-11-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0262-2023

## Citation

> AI Analytics. FDA recall Z-0262-2023. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0262-2023. Source: US FDA. Licensed CC0.

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