FDA recall Z-0791-2019

3M Company - Health Care Business · Class II · device

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

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

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0791-2019