FDA Device recall Z-1185-2017
Junction Box - 1104343 and 1193560
- FDA Device
- Class II
- terminated
- Published 2017-02-15
On 2017-02-15 the FDA classified a Class II recall of Junction Box - 1104343 and 1193560 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-1185-2017 |
| 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
Junction Box - 1104343 and 1193560
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 | 16FF017240 16EF024702 16EF024703 16EF022151 16EF022152 16EF022153 16EF023728 16FF017238 16FF017239 16EF024693…16FF017240 16EF024702 16EF024703 16EF022151 16EF022152 16EF022153 16EF023728 16FF017238 16FF017239 16EF024693 16EF024694 16FF019751 16EF014948 16EF018634 16EF018635 16EF018636 16FF017229 16FF017230 16EF022150 16EF032147 16EF032148 16EF032149 16EF032150 16EF032151 16EF032152 16FF015954 16FF015955 16FF015956 16FF015957 16EF018630 16EF018631 16EF034256 16EF022146 16EF022147 16EF018623 16FF017236 16EF032132 16EF027693 16EF027694 16EF029506 16EF027688 16EF027692 16EF029504 16EF024695 16FF019752 16FF019753 16EF029516 16EF029517 16EF029518 16EF029519 16EF014963 16EF024698 16EF024700 16EF024701 16FF022168 16EF016093 16EF023719 16FF022161 16FF022165 16EF024708 16FF017237 16EF027705 16EF023726 16EF014950 16EF014952 16EF011961 16EF011962 16EF011963 16EF011964 16EF014951 16EF018625 16EF018626 16EF018627 16EF018628 16EF018629 16EF022135 16EF022136 16EF022137 16EF022138 16EF022139 16FF015963 16FF015964 16FF015965 16FF |
|---|
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-1185-2017%22
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