FDA recall record

Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended recall — FDA Z-2433-2015

Charging base of surgical clippers overheats and smokes.

Class IIclassification
Z-2433-2015official record ID
Aug 26, 2015report date

Recall record at a glance

Official recordZ-2433-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedline Industries Inc.
Report dateAug 26, 2015
Recall initiation dateJul 8, 2015
Quantity7062 units (U.S.); 540 units Foreign
LocationMundelein, IL, United States

Official product description

Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended for the removal of body hair from patients as required prior to surgery or other minor procedures.

Why the product was recalled

Charging base of surgical clippers overheats and smokes.

Distribution information

Worldwide Distribution - US (nationwide) Distribution including Puerto Rico and to the countries of : United Arab Emirates, Barbados, Bahamas, Chile, Costa Rica, Italy, Lebanon, and Singapore.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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