Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

PR1000 Pivot Rehab Bed AC powered adjustable bed. Recalled by Med-Mizer, Inc. Due to Under certain conditions, when pivoting bed to the...

Date: July 25, 2018
Company: Med-Mizer, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Med-Mizer, Inc. directly.

Affected Products

PR1000 Pivot Rehab Bed AC powered adjustable bed.

Quantity: 230 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 28 states: AZ, AR, FL, GA, ID, IL, IN, IA, KY, ME, MI, MN, MO, NE, NM, NY, NC, ND, OH, OK, PA, SC, SD, TN, TX, VA, WA, WI

Affected (28 states)Not affected

About Med-Mizer, Inc.

Med-Mizer, Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report