Skip to content
Recall Observatory FDA recall evidence

Device product

3M Surgical Clipper Professional 9681

Z-0777-2018

February 02, 2018

Class II

Product summary

Firm
3M Company - Health Care Business
Event
Event 79289
Status
Terminated
Classification
Class II
Quantity
120000 units
Official record key
device-enforcement:Z-0777-2018

Official wording

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.

Code information: all

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.