[Recalled] E.CAM emission computed tomography system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with e
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | E.CAM emission computed tomography system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV. |
|---|---|
| Brand / manufacturer | Siemens Medical Solutions USA, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1297-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 11 April 2012 |
| EAN / barcode | 402700069 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Radial motor drives replaced during a customer service action were incorrectly assembled backwards.
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 Siemens Medical Solutions USA, Inc.
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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