RegWardenFDA facility compliance records
Recall

Class II — Wahl Clipper Corp

Recalling firmWahl Clipper Corporation
Registered facilityView this company's 2 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonThe connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard
ProductWAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
Quantity161 units
DistributionUS Nationwide distribution including in the states of CT, FL, UT, MO, WI, FL, CA, IL, PA.
Initiated2020-12-15
Classified2021-02-05
Terminated2023-05-09
Recall numberZ-1084-2021
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Wahl Clipper Corp (Z-1084-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87229/

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