Reported Apr 24, 2024 · Ongoing

Achieva 3.0TX for PET, Magnetic Resonance System.

Philips North America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • Achieva 3.0TX for PET, Magnetic Resonance System.
Lot codes and dates
    • Model No. 781479
    • UDI-DI n/a
    • Serial No. 43102
Amount recalled
1 unit

This recall covers 41 products

The agency filed one notice per product. You are reading one of them; the other 40 are below.

28 more are in the archive.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

Patient support table floor plate may be incorrectly installed.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Philips North America LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.