FDA Medical Device Recalls (openFDA)
Medline Industries Inc: 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 number
- Z-2756-2019
- Recalling firm
- Medline Industries Inc
- 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.
- Status
- Open, Classified
- Initiated
- 2019-09-06
- Posted
- not on file
- Terminated
- not on file
- 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.
- Root cause
- Process control
- 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.
- Quantity
- 500 units
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- 14G1
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LWK
- Firm FEI
- 1417592
- Firm city
- Northfield
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28