Facility

KARMAN HEALTHCARE INC.

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)	1000306460
Establishment type	Repack or Relabel Medical Device
Location	19255 San Jose Ave CITY OF INDUSTRY, CA, US 91748
Registration status	Active · expires 2026
Parent company	KARMAN HEALTHCARE, INC. (owner-operator 9011011)
Brand names	Karman

Activity by year

Recalls (1)

Devices registered here (1)

Armrest, Wheelchair
Product code IML (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3920

Recalls & enforcement

Class IITerminated2016-01-27
Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.

All facilities operated by KARMAN HEALTHCARE, INC.

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. “KARMAN HEALTHCARE INC. (FEI 1000306460) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000306460-karman-healthcare-inc/

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