Karma Flexx Wheelchair Manual Wheelchair recall
Karma Flexx Wheelchair Manual Wheelchair.
Why was Karma Flexx Wheelchair Manual Wheelchair recalled?
Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Karma Flexx Wheelchair Manual Wheelchair.
- Recalling firm
- Karman Healthcare Inc
- Quantity
- 35
- Distribution
- U.S. distribution to the following states -- WA, CA, NY, and TX.
- Recall date
- March 9, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)