medical MODERATE Updated 2017-02-15

Invacare Corporation recalls Foot Section - BAR5490IVC

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Recalled Product

Foot Section - BAR5490IVC

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Hazard / Issue

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

Issued by

FDA

Affected 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, WI
Lot/Code Info: BAR5490IVC

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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