FDA Medical Device Recalls (openFDA)
Wahl Clipper Corp: WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
- Recall number
- Z-1084-2021
- Recalling firm
- Wahl Clipper Corp
- Product
- WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
- Status
- Terminated
- Initiated
- 2020-12-15
- Posted
- 2021-02-05
- Terminated
- 2023-05-09
- Reason
- The connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard
- Root cause
- 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
- 161 units
- Distribution
- US Nationwide distribution including in the states of CT, FL, UT, MO, WI, FL, CA, IL, PA.
- Lot, serial or model codes
- all lots
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ISA
- Firm FEI
- 1410825
- Firm city
- Sterling
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28