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FDAFDA · Food and drugs·Recall number Z-1182-2017

Bariatric Bed - BAR600IVC

Published February 15, 2017 · Recall initiated: December 2, 2016

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

The junction box used in the bariatric bed may emit sparks and result in a fire.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Invacare Corporation
Distributor
Products were distributed in the following states: AK, AL, AR, CA, CO, CT, FL, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI. No foreign accounts
Lot
BAR600IVC
Risk classification
Class II
Area (FDA)
device
Country
United States

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