FDA Device recall Z-0777-2018
3M Surgical Clipper Professional 9681
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of 3M Surgical Clipper Professional 9681 by 3m Health Care Business, citing failure to follow proper charging practices can result in lithium-ion battery degradation, characterized by excessive heat during operation or failure to properly charge. In rare….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0777-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-02 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | 3m Health Care Business |
| Distribution | US |
Product
3M Surgical Clipper Professional 9681
Reason
Failure to follow proper charging practices can result in lithium-ion battery degradation, characterized by excessive heat during operation or failure to properly charge. In rare circumstances, battery degradation has been associated with battery venting, which is a rapid release of battery energy.
Identifiers
| code_info | all |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0777-2018%22
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