Recall Z-2756-2019— Medline Industries Inc
Class II · Ongoing
Class II FDA medical device recall by Medline Industries Inc, initiated 2019-09-06. FDA's recall record names no specific 510(k) clearance for this event. Product: 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: 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..
- Recalling firm
- Medline Industries Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2019-09-06
- Firm location
- Northfield, IL, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.