# FDA recall Z-1084-2021

> **Wahl Clipper Corp** · Class II · device recall initiated 2020-12-15.

## Product

WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.

## Reason for recall

The connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard

## Distribution

US Nationwide distribution including in the states of CT, FL, UT, MO, WI, FL, CA, IL, PA.

## Key facts

- **Recall number:** Z-1084-2021
- **Recalling firm:** Wahl Clipper Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-15
- **Report date:** 2021-02-17
- **Termination date:** 2023-05-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1084-2021

## Citation

> AI Analytics. FDA recall Z-1084-2021. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-1084-2021. Source: US FDA. Licensed CC0.

---

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