Junction Box — Class II medical device recall Z-1185-2017
Terminated recall by Invacare Corporation, reported 2017-02-15, distributed in AK, AL, AR, CA, CO, CT, FL, HI…. A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into
| Recall number | Z-1185-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2016-12-02 |
| Classified | 2017-02-09 |
| Reported by FDA | 2017-02-15 |
| Terminated | 2017-11-02 |
| Distributed | 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 |
| Quantity | 161 units |
Product
Junction Box - 1104343 and 1193560
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1185-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.