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Med-Mizer, Inc. recalls PR1000 Pivot Rehab Bed AC powered adjustable bed.
Recalled September 26, 2018 · FDA recall Z-3183-2018 · Med-Mizer
Hazard
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 · FDA Class II
Units
230 units
Sold at
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.
Description
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
Product
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Manufacturer(s)
Med-Mizer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →