Philips North America Llc recalls DigitalDiagnost C50 1.1
Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of the image on the first examination due to an issue in…
Read the official notice →- Date
- 2022-09-07
- Country
- United States
- Brand
- Philips
- Product
- DigitalDiagnost C50 1.1
- Classification
- Class II
- Units
- Nationwide Distribution including Puerto Rico
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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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