Z-0860-2016 Class II Terminated
FDA device recall Z-0860-2016 was initiated by Hill-Rom, Inc. on Jan 20, 2016 and is designated Class II. Reason for recall: The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury. The recall status is terminated (terminated Feb 7, 2017). Affected quantity: 216.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 2, 2016
- Initiation Date
- Jan 20, 2016
- Termination Date
- Feb 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 216
Product Description
Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to provide an aesthetically pleasing design that will enhance the overall experience for the bariatric patient. Using spring box construction and an exceptionally smooth mechanism, the patient is able to move into a reclined position with little effort and infinite positions up to 38 degrees. An independent footrest enables patients to be in a fully seated position with their feet up for added comfort.
Reason for Recall
The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury.
Distribution Pattern
Worldwide Distribution - US including AL, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, VT, WA, WI, WV, WY, VA Medical Center and Internationally to Canada and Mexico. **Consumer Recommended Depth - Consumers/User**
Code Information
Bariatric Power Recliner, Product Model # P9096; all power bariatric chairs that are affected by this field action is distributed within the following serial number range: L341RW9151 through P070RW0812
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0860-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026