Philips North America Llc recalls SENSE Breast Coil 3.0T 7ch
- Recall date
- November 4, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0546-2025
- FDA classification
- Class II
- Brand / firm
- Philips North America Llc
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
SENSE Breast Coil 3.0T 7ch
Get recall alerts
Free email alert whenever Philips North America Llc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Philips North America Llc