Mammotrak Diagnostic Coil 1.5T
Reported: December 4, 2024 Initiated: November 4, 2024 #Z-0541-2025
Product Description
Mammotrak Diagnostic Coil 1.5T
Reason for Recall
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 5,231 units
- Distribution
- US Nationwide distribution.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
Mammotrak Diagnostic Coil 1.5T. Recalled by Philips North America Llc. Units affected: 5,231 units.
Why was this product recalled? ▼
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 4, 2024. Severity: Moderate. Recall number: Z-0541-2025.
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