Z-3183-2018 Class II Terminated

Recalled by Med-Mizer, Inc. — Batesville, IN

Recall Details

Product Type
Devices
Report Date
September 26, 2018
Initiation Date
July 25, 2018
Termination Date
October 11, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
230 units

Product Description

PR1000 Pivot Rehab Bed AC powered adjustable bed.

Reason for Recall

Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made

Distribution Pattern

The products were distributed to the following US states: AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI. The products were distributed to the following foreign countries: Canada, China, and Denmark.

Code Information

ALL Pivot Rehab PR1000 Beds built between 12/01/2010 thru 12/22/2014 SN: PR 10001 build date 12/01/2010 thru PR 10255 build date 12/22/2014