Data Foundry

Medical device recalls 2016

Hill-Rom Bariatric Power Recliner — Class II medical device recall Z-0860-2016

Terminated recall by Hill-Rom, Inc., reported 2016-03-02, distributed in AL, AZ, CA, CO, CT, FL, GA, HI…. The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer

Recall numberZ-0860-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHill-Rom, Inc., Batesville, IN, United States
Recall initiated2016-01-20
Classified2016-02-23
Reported by FDA2016-03-02
Terminated2017-02-07
DistributedAL, 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
Countries outside the USCA, MX
Quantity216
Model numbers660, P9096

Product

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0860-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.