Skip to content
Recall Observatory FDA recall evidence

Device product

Karma Flexx Wheelchair Manual Wheelchair.

Z-1025-2016

January 27, 2016

Class II

Product summary

Firm
Karman Healthcare Inc
Event
Event 73159
Status
Terminated
Classification
Class II
Quantity
35
Official record key
device-enforcement:Z-1025-2016

Official wording

Reason: Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.

Code information: Item # 935-0245H6 Flexx (KM852216) Serial # TM14-A03982-TM14-A03991 Item # 935-0246H6 Flexx (KM852218) Serial # TM14-A03992-TM14-A04012 Item # 935-0247H6 Flexx (KM852220) Serial # TM14-A4013-TM14-A04017

Distribution pattern: U.S. distribution to the following states -- WA, CA, NY, and TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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

Field note

Send feedback

We'll only use this to respond to your feedback.