Invacare Corporation: Medical Device Recall in 2017 - (Recall #: Z-1184-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Foot Section - BAR5490IVC

Product Classification:

Class II

Date Initiated: December 2, 2016

Date Posted: February 15, 2017

Recall Number: Z-1184-2017

Event ID: 75939

Reason for Recall:

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

Status: Terminated

Product Quantity: 292 units

Code Information:

BAR5490IVC

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated