Z-1020-2015 Class II Terminated
FDA device recall Z-1020-2015 was initiated by Sunrise Medical (US) LLC on December 19, 2014 and is designated Class II. Reason for recall: There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs. The recall status is terminated (terminated March 10, 2015). Affected quantity: 6.
Recall Details
- Product Type
- Devices
- Report Date
- February 4, 2015
- Initiation Date
- December 19, 2014
- Termination Date
- March 10, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6
Product Description
Quickie Q7 Adult Rigid Wheelchair Model EIR4.
Reason for Recall
There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.
Distribution Pattern
Nationwide Distribution in the states of CO and ME.
Code Information
Serial numbers: R4-025066, R4-025051, R4-025010, R4-024771, R4-024738, R4-024649.