Reported Apr 24, 2024 · Ongoing
Ingenia Ambition X, 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?
- Ingenia Ambition X, Magnetic Resonance System.
- Lot codes and dates
410 of 410 codes
Model No. 781359782109782138UDI-DI 884838090040884838098350884838108622Serial No. 471994729047387470624732547038475544704347004472784732347027475424779447045473364733147282470934718547606471834709047198473244721047862477004721647066470294732247051470284720347659473354725347289470224735147759470444706347061470544737747316473714737047380470074719647204
- Amount recalled
- 404 units
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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.