Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due to Potential safety issue where a patient may be...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America Llc directly.
Affected Products
Mammotrak Interventional Coil 1.5T
Quantity: 5,231 units
Why Was This Recalled?
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report