3M Surgical Clipper Professional 9681
Reported: March 7, 2018 Initiated: February 2, 2018 #Z-0777-2018
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.
Details
- Recalling Firm
- 3M Company - Health Care Business
- Units Affected
- 120000 units
- Distribution
- 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.
- Location
- Saint Paul, MN
Frequently Asked Questions
What product was recalled? ▼
3M Surgical Clipper Professional 9681. Recalled by 3M Company - Health Care Business. Units affected: 120000 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 7, 2018. Severity: Moderate. Recall number: Z-0777-2018.
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