Z-2402-2016 Class II Terminated
FDA device recall Z-2402-2016 was initiated by Invacare Corporation on March 15, 2016 and is designated Class II. Reason for recall: The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They discovered that the Junction Box may omit sparks which could result in a fire in the presenc… The recall status is terminated (terminated September 15, 2017). Affected quantity: 1,011 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 17, 2016
- Initiation Date
- March 15, 2016
- Termination Date
- September 15, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,011 units
Product Description
Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
Reason for Recall
The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They discovered that the Junction Box may omit sparks which could result in a fire in the presence of flammable materials.
Distribution Pattern
US Nationwide Distribution including DC and PR. Internationally Canada.
Code Information
Model #'s:1104343 & 1104345