Z-1116-2014 Class II Terminated
FDA device recall Z-1116-2014 was initiated by Winco Mfg., LLC on September 6, 2013 and is designated Class II. Reason for recall: A supplier manufacturing assembly defect with the right hand recline mechanism. Use of this product may result in the loss of functionality of the three (3) position lock bar when in a reclined positi… The recall status is terminated (terminated December 30, 2014). Affected quantity: 369 units (all models).
Recall Details
- Product Type
- Devices
- Report Date
- March 5, 2014
- Initiation Date
- September 6, 2013
- Termination Date
- December 30, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 369 units (all models)
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution - USA nationwide including Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kanas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin, West Virginia, Puerto Rico and Internationally to the country of Canada.