Reported Feb 15, 2017 · Terminated

Foot Section - BAR5490IVC

Invacare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Invacare Corporation · 1 Invacare Way · Elyria, OH · 44035-4190

Is this the product you have?

  • Foot Section - BAR5490IVC
Lot codes and dates
  • BAR5490IVC
Amount recalled
292 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 2, 2017 · Data as of Sep 19, 6:13 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.