# FDA recall Z-2756-2019

> **Medline Industries Inc** · Class II · device recall initiated 2019-09-06.

## 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.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2756-2019
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-09-06
- **Report date:** 2019-10-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2756-2019

## Citation

> AI Analytics. FDA recall Z-2756-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2756-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*