FDA Device Recall
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
- Recall Number
- Z-2988-2026
- CFRES ID
- 221719
- Firm
- Philips Healthcare (Suzhou) Co., Ltd.
- Status
- Open, Classified
- Initiated
- Jun 26, 2026
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Source: https://healthaicentral.com/research/regulatory-clearance/recalls/221719