Recalls / —

—#210877

Product

Mammotrak Interventional Coil 1.5T

FDA product code

MOS — Coil, Magnetic Resonance, Specialty

Device class

Class 2

Medical specialty

Radiology

510(k) numbers

K032576

Affected lot / code info

REF: 453530228882; UDI-DI: 00884838066779; Serial No. 69, 82, 143, 64, 77, 87, 76, 81, 134, 124, 141, 103, 135, 138, 73, 72, 131.

Why it was recalled

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Root cause (FDA determination)

Use error

Action the firm took

An URGENT MEDICAL DEVICE CORRECTION notice dated 10/31/24 was mailed to consignees. Consignees are to continue using affected systems in accordance with the intended use. When using the system follow section PRECAUTIONS, CAUTIONS & WARNINGS in the Instructions For Use (IFU). Consignees are to circulate the recall notice to all users for their awareness of the potential issue. The Recall Response Form is to be provided back to Philips MR within 30 days at Philips.Recall@philips.com. Customers with any questions are to contact their local Philips Representative.

Recalling firm

Firm

Philips North America Llc

Address

222 Jacobs St, Cambridge, Massachusetts 02141-2289

Distribution

Distribution pattern

US Nationwide distribution.

Timeline

Recall initiated

2024-11-04

Posted by FDA

2024-11-25

Status

—

Source: openFDA Device Recall endpoint. Recall record ID #210877. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.