Data Foundry

Medical device recalls 2021

WAHL 4212 HEATED MASSAGER — Class II medical device recall Z-1084-2021

Terminated recall by Wahl Clipper Corp, reported 2021-02-17, distributed nationwide. The connection between the massager and heat element can overheat causing smoke or spark, which may pose a fir

Recall numberZ-1084-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmWahl Clipper Corp, Sterling, IL, United States
Recall initiated2020-12-15
Classified2021-02-05
Reported by FDA2021-02-17
Terminated2023-05-09
DistributedNationwide (US)
Quantity161 units
Reason classesdevice malfunction

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

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-1084-2021. 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.