Class II — 3M Company - Health Care Business
| Recalling firm | 3M COMPANY |
|---|---|
| Registered facility | View this company's 13 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| 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. |
| Quantity | 19,860 units |
| Distribution | US Distribution and countries Brazil and Canada. |
| Initiated | 2019-01-14 |
| Classified | 2019-01-30 |
| Terminated | 2021-02-11 |
| Recall number | Z-0791-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — 3M Company - Health Care Business (Z-0791-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81933/
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