FDA Device recall Z-1184-2017
Foot Section - BAR5490IVC
- FDA Device
- Class II
- terminated
- Published 2017-02-15
On 2017-02-15 the FDA classified a Class II recall of Foot Section - BAR5490IVC by Invacare, citing A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1184-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-12-02 |
| Published | 2017-02-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Invacare |
| Distribution | 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 |
Product
Foot Section - BAR5490IVC
Reason
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
Identifiers
| code_info | BAR5490IVC |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1184-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.