Med-Mizer, Inc.: Medical Device Recall in 2018 - (Recall #: Z-3183-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

PR1000 Pivot Rehab Bed AC powered adjustable bed.

Product Classification:

Class II

Date Initiated: July 25, 2018

Date Posted: September 26, 2018

Recall Number: Z-3183-2018

Event ID: 80832

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

Status: Terminated

Product Quantity: 230 units

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

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.

Voluntary or Mandated:

Voluntary: Firm initiated