Reported Apr 24, 2024 · Ongoing
Ingenia Ambition S, 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 S, Magnetic Resonance System.
- Lot codes and dates
351 of 351 codes
Model No. 782133782139781359782108UDI-DI 884838090057884838098343884838108639Serial No. 4864648700482374866548179481204864548252482174864848708481624868848035486564828748719485524828648588486084866948015481714874948274480524800048001480034853548004480054800948011480104801248014480184801648017480194802248023480324802648030480344803748036480204804048044
- Amount recalled
- 344 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.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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