Karman Healthcare Inc: Medical Device Recall in 2016 - (Recall #: Z-1025-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Karma Flexx Wheelchair Manual Wheelchair.

Product Classification:

Class II

Date Initiated: January 27, 2016

Date Posted: March 9, 2016

Recall Number: Z-1025-2016

Event ID: 73159

Reason for Recall:

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

Status: Terminated

Product Quantity: 35

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.

Voluntary or Mandated:

Voluntary: Firm initiated