Z-0791-2019 Class II Terminated
FDA device recall Z-0791-2019 was initiated by 3M Company - Health Care Business on January 14, 2019 and is designated Class II. 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. The recall status is terminated (terminated February 11, 2021). Affected quantity: 19,860 units.
Recall Details
- Product Type
- Devices
- Report Date
- February 6, 2019
- Initiation Date
- January 14, 2019
- Termination Date
- February 11, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 19,860 units
Product Description
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 Pattern
US Distribution and countries Brazil and Canada.
Code Information
all lots