Z-0274-2016 Class II Terminated
FDA device recall Z-0274-2016 was initiated by Hill-Rom, Inc. on Oct 7, 2015 and is designated Class II. Reason for recall: Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints of patient injury when exiting the beds set at the lowest position setting. The recall status is terminated (terminated Feb 10, 2017). Affected quantity: 12251 units.
Recall Details
- Product Type
- Devices
- Report Date
- Nov 25, 2015
- Initiation Date
- Oct 7, 2015
- Termination Date
- Feb 10, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 12251 units
Product Description
Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed
Reason for Recall
Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints of patient injury when exiting the beds set at the lowest position setting.
Distribution Pattern
Worldwide Distribution - USA (nationwide) to the states of : AL, AR, AZ. CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WI and WV., and to the countries of : Canada and France.
Code Information
Product # P3930A; Dates of Manufacture 5-DEC-2007 to 14-SEP-2015; Serial numbers from I325AR0038 thru Q257AR2299
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0274-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026