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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.

FDA Recall Z-2756-2019 · Posted None

Recalling FirmMedline Industries Inc
Recall StatusOpen, Classified
Product CodeLWK
Date Initiated2019-09-06
Product Quantity500 units

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.

Firm 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.

Root Cause

Process control

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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