FDAFDA · Food and drugs·Recall number Z-0277-2024
DigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digital radiographic images.
Published November 15, 2023 · Recall initiated: September 21, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for units suspended on the ceiling to fail and fall.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Philips North America Llc
- Distributor
- Nationwide distribution.
- Lot
- Model No. 712025; Serial No. SN13000328.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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