Facility

WAHL CLIPPER CORP.

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1410825
Establishment type	Repack or Relabel Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	2900 NORTH LOCUST ST. Sterling, IL, US 61081
Registration status	Active · expires 2026
Parent company	Wahl Clipper Corporation (owner-operator 1410825)

Activity by year

Recalls (1)

Devices registered here (1)

Razor, Surgical
Product code LWK (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800

Recalls & enforcement

Class IITerminated2020-12-15
The connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard

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

Cite this record

RegWarden. “WAHL CLIPPER CORP. (FEI 1410825) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1410825-wahl-clipper-corp/

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