PHILIPS HEADQUARTERS CAMBRIDGE recalls Incisive CT- whole-body computed tomography (CT) X-Ray System Model Number: 728144
- Recall date
- April 12, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1622-2023
- FDA classification
- Class II
- Brand / firm
- PHILIPS HEADQUARTERS CAMBRIDGE
- Sold / distributed
- AR, CA, OK, TX Foreign: Country Argentina Australia Austria China Colombia Czech Republic Dominican Rep France Germany Guadeloupe Hong Kong India Japan Kuwait Latvia Lithuania Netherlands Norway Portugal Romania Spain Switzerland Taiwan Thailand United Kingdom Vietnam
Why it was recalled
Potential for Incorrect Image Orientation resulting images may be flipped or reversed result in misdiagnosis, incorrect treatment of a condition, or additional radiation exposure if a rescan is required
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Incisive CT- whole-body computed tomography (CT) X-Ray System Model Number: 728144
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