[Recalled] Mammotrak Interventional Coil 3.0T — Potential safety issue where a patient may be harmed while preparing for or dur… | FDA 2024-11-04

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Potential safety issue where a patient may be harmed while preparing for or during a scan.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Philips North America Llc

• DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images. — Class II
• Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device REF: 782116 — Class II
• IntelliVue MP90. Product Number: M8010A. — Class II
• IntelliVue MP30. Product Number: M8002A. — Class II
• Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity , Adt/Pedi Intub CO2 Line LTerm Lng , Adt/Pedi Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line LTerm , Neo/Inf Intub CO2 L — Class II
• Ingenia 1.5T S, Magnetic Resonance System. — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.