Recall Z-0777-2018— 3M Company - Health Care Business
Class II · Terminated
Class II FDA medical device recall by 3M Company - Health Care Business, initiated 2018-02-02, terminated 2024-08-02. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- 3M Company - Health Care Business
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-02-02
- Terminated
- 2024-08-02
- Firm location
- Saint Paul, MN, United States
Product description
3M Surgical Clipper Professional 9681
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.