FDA Device Recall
Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
- Recall Number
- Z-0640-2024
- CFRES ID
- 204881
- Firm
- Philips Healthcare (Suzhou) Co., Ltd. Suzhou Industrial Park No.
- Status
- Open, Classified
- Initiated
- Dec 23, 2022
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Source: https://healthaicentral.com/research/regulatory-clearance/recalls/204881