PHILIPS MEDICAL SYSTEMS recalls CombiDiagnost R90 1.1 (709031)
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image…
Read the official notice →- Date
- 2024-02-21
- Country
- United States
- Brand
- Philips Medical Systems
- Product
- CombiDiagnost R90 1.1 (709031)
- Classification
- Class II
- Units
- US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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