Z-2433-2015 Class II Terminated
FDA device recall Z-2433-2015 was initiated by Medline Industries Inc on Jul 8, 2015 and is designated Class II. Reason for recall: Charging base of surgical clippers overheats and smokes. The recall status is terminated (terminated Nov 29, 2017). Affected quantity: 7062 units (U.S.); 540 units Foreign.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 26, 2015
- Initiation Date
- Jul 8, 2015
- Termination Date
- Nov 29, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7062 units (U.S.); 540 units Foreign
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.
Reason for Recall
Charging base of surgical clippers overheats and smokes.
Distribution Pattern
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.
Code Information
Product item number: DYND70800 with Lot Numbers: 13F1, 13KD, 14A1, 14C1, and Lot 1.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2433-2015
- openFDA file date
- Oct 27, 2026
- Loaded by RegDataLab
- Oct 29, 2026