3M — Class II medical device recall Z-0791-2019
Terminated recall by 3M Company - Health Care Business, reported 2019-02-06. 3M has recently received reports involving the 3MTM Surgical Clipper by Remington¿, Model 9602, overheating in
| Recall number | Z-0791-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2019-01-14 |
| Classified | 2019-01-30 |
| Reported by FDA | 2019-02-06 |
| Terminated | 2021-02-11 |
| Countries outside the US | BR, CA |
| Quantity | 19,860 units |
| Reason classes | device malfunction |
| Model numbers | 9602 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0791-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.