Z-2756-2019 Class II Ongoing
FDA device recall Z-2756-2019 was initiated by Medline Industries Inc on September 6, 2019 and is designated Class II. Reason for recall: The recall is being conducted due to a potential defective component on the circuit board causing the charger base to overheat which could result in a charger base malfunction. The recall status is ongoing. Affected quantity: 500 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 2, 2019
- Initiation Date
- September 6, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 500 units
Product Description
MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.
Reason for Recall
The recall is being conducted due to a potential defective component on the circuit board causing the charger base to overheat which could result in a charger base malfunction.
Distribution Pattern
US Nationwide Distribution
Code Information
14G1