[Recalled] Junction Box - 1104343 and 1193560 — A quality issue with the junction box used in the bariatric bed junction that m… | FDA 2016-12-02
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Junction Box - 1104343 and 1193560 |
|---|---|
| Brand / manufacturer | Invacare Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1185-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 02 December 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Invacare Corporation
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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