FDA Recall Open, Classified

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.

Recall: Z-2756-2019 · Initiated September 6, 2019

Recall

Recall Number
Z-2756-2019
Event Number
83740
Firm
Medline Industries Inc
FEI Number
1417592
Product Code
LWK
Status
Open, Classified
Root Cause
Process control
Initiated
September 6, 2019
Address
Three Lakes Drive, Northfield, IL, 60093

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

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.

Action

Medline Industries initiated the recall on 09/06/2019 by letter. The letter identified the affected product, problem and actions to be taken. The letter instructed customers to: 1. Immediately check your stock for the affected item number and lot number listed on the destruction form. Quarantine all affected product. Destroy all product belonging to the affected lot numbers listed on the destruction form. 2. Please return the completed enclosed destruction form listing the quantity of affected product destroyed. Even if you do not have any affected product please complete and return the form. For questions contact 866-359-1704.

Distribution

US Nationwide Distribution

Quantity

500 units