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U.S. Department of Health and Human Services

Class 2 Device Recall WAHL 4212 HEATED MASSAGER

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  Class 2 Device Recall WAHL 4212 HEATED MASSAGER see related information
Date Initiated by Firm December 15, 2020
Date Posted February 05, 2021
Recall Status1 Terminated 3 on May 09, 2023
Recall Number Z-1084-2021
Recall Event ID 87229
Product Classification Massager, therapeutic, electric - Product Code ISA
Product WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
Code Information all lots
Recalling Firm/
Manufacturer		 Wahl Clipper Corp
2902 Locust St
Sterling IL 61081
For Additional Information Contact Colleen Butts
815-548-8356
Manufacturer Reason
for Recall		 The connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard
FDA Determined
Cause 2		 Device Design
Action Wahl initiated the recall on 12/15/2020 to its direct consignee by email and posted a notice on its website www.fda.gov on 12/23/2020. The firm is requesting the return of the units.
Quantity in Commerce 161 units
Distribution US Nationwide distribution including in the states of CT, FL, UT, MO, WI, FL, CA, IL, PA.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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