MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE — Class II medical device recall Z-2756-2019
Ongoing recall by Medline Industries Inc, reported 2019-10-02, distributed nationwide. The recall is being conducted due to a potential defective component on the circuit board causing the charger
| Recall number | Z-2756-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2019-09-06 |
| Classified | 2019-09-26 |
| Reported by FDA | 2019-10-02 |
| Distributed | Nationwide (US) |
| Quantity | 500 units |
| Reason classes | device malfunction |
| Model numbers | DYND70800 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2756-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.