# FDA recall Z-0791-2019

> **3M Company - Health Care Business** · Class II · device recall initiated 2019-01-14.

## Product

3M(TM) Surgical Clipper by Remington(R) REF 9602    The 3M Surgical Clipper Classic, 9602, is intended to remove body hair and head hair from patients in preparation for any medical procedure requiring hair removal.

## Reason for recall

3M has recently received reports involving the 3MTM Surgical Clipper by Remington¿, Model 9602, overheating in mobile/field EMS situations while charging from a modified sine wave power inverter.

## Distribution

US Distribution and countries Brazil and Canada.

## Key facts

- **Recall number:** Z-0791-2019
- **Recalling firm:** 3M Company - Health Care Business
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-14
- **Report date:** 2019-02-06
- **Termination date:** 2021-02-11

- **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-0791-2019

## Citation

> AI Analytics. FDA recall Z-0791-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0791-2019. Source: US FDA. Licensed CC0.

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