Philips Healthcare recalls CombiDiagnost R90 is multi-functional general R/F systems.
The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards. This includes the Radiation Warning Label [21CFR 1020.30 (j)] and…
Read the official notice →- Date
- 2021-12-01
- Country
- United States
- Brand
- Philips Healthcare
- Product
- CombiDiagnost R90 is multi-functional general R/F systems.
- Classification
- Class II
- Units
- US Nationwide Distribution
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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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- Ask the pharmacy or supplier about a replacement or refund.
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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