Z-0777-2018 Class II Terminated
FDA device recall Z-0777-2018 was initiated by 3M Company - Health Care Business on Feb 2, 2018 and is designated Class II. 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… The recall status is terminated (terminated Aug 2, 2024). Affected quantity: 120000 units.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 7, 2018
- Initiation Date
- Feb 2, 2018
- Termination Date
- Aug 2, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 120000 units
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.
Distribution Pattern
Worldwide distribution including US nationwide, including Puerto Rico. Singapore, Australia, Canada, Chile, Colombia, Costa Rica, Brazil, Dominica, Ecuador, Guatemala, UAE, Israel, Japan, Korea, Mexico, new Zealand, Paraguay, Peru, Taiwan, Uruguay, India, Bolivia, El Salvador, Saudi Arabia, and Thailand.
Code Information
all
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0777-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026