[Recalled] MXR-35 Diagnostic X-ray High Voltage Generator manufactured by DRGEM Corporation. x-ray generator — The MXR-35 X-ray Generator's labeling did not include the certification stateme… | FDA 2012-06-29
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | MXR-35 Diagnostic X-ray High Voltage Generator manufactured by DRGEM Corporation. x-ray generator |
|---|---|
| Brand / manufacturer | Fujifilm Medical System USA, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1642-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 29 June 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The MXR-35 X-ray Generator's labeling did not include the certification statement as required by 21 CFR Part 10 10.2.
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 →
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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