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Philips North America Llc recalls dS Breast 7ch 3.0T
Recalled December 4, 2024 · FDA recall Z-0540-2025 · Philips North America
Hazard
Potential safety issue where a patient may be harmed while preparing for or during a scan. · FDA Class II
Units
5,231 units
Sold at
US Nationwide distribution.
Description
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Product
dS Breast 7ch 3.0T
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →