FDA recall record

Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric recall — FDA Z-0860-2016

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

Class IIclassification
Z-0860-2016official record ID
Mar 2, 2016report date

Recall record at a glance

Official recordZ-0860-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHill-Rom, Inc.
Report dateMar 2, 2016
Recall initiation dateJan 20, 2016
Quantity216
LocationBatesville, IN, United States

Official 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.

Why the product was recalled

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

Distribution information

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**

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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