Med-Mizer, Inc. recalls PR1000 Pivot Rehab Bed AC powered adjustable bed.

Recall date

July 25, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-3183-2018

FDA classification

Class II

Brand / firm

Med-Mizer, Inc.

Sold / distributed

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.

Why it was 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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

PR1000 Pivot Rehab Bed AC powered adjustable bed.