FDA Medical devices recall ·
Mammotrak Diagnostic Coil 1.5T recall
- Recall number
- Z-0541-2025
- Date
- (initiated November 4, 2024)
- Company / brand
- Philips North America Llc
222 Jacobs St, Cambridge, MA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 5,231 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Mammotrak Diagnostic Coil 1.5T
Why was it recalled?
Potential safety issue where a patient may be harmed while preparing for or during a scan.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
REF: 453530228872; UDI-DI: 00884838066762; Serial No. 79, 124, 71, 179, 124, 182, 45, 43, 178, 171, 181, 53, 40, 52, 69, 187, 95.
Distribution
US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0541-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.