Medical device recalls Moderate risk

Hill-Rom, Inc. recalls Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to pro…

Recall date
January 20, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0860-2016
FDA classification
Class II
Brand / firm
Hill-Rom, Inc.
Sold / distributed
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…

Why it was recalled

The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

Get recall alerts

Free email alert whenever Hill-Rom, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Hill-Rom, Inc.