RecallDepth

PR1000 Pivot Rehab Bed AC powered adjustable bed.

Company
Med-Mizer, Inc.
Recall Initiated
July 25, 2018
Terminated
October 11, 2019
Recall Number
Z-3183-2018
Quantity
230 units
Firm Location
Batesville, IN

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

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.

Lot / Code Info

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

Root Cause

Device Design

Action Taken

Customers were contacted via telephone on 7/25/18 to notify them of the issue and to make them aware of the correction. Customers were then mailed a notification letter along with necessary parts.

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