Reported Nov 29, 2023 · Ongoing
Intera 1.5T
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?
- Intera 1.5T
- Lot codes and dates
- Product No. 781195 & 781295
- UDI-DI
103 of 103 codes
N/ASerial No. 1851018516185291855018564185671857818583185921865718660186671867818701187091871118714187251872718769187731877618787188121882018854188561885718870188731887818884188891889018905189061890718913189171892018923189311893518947189481895018965189731898618998204022040320404204092042620441300043003030037
- Amount recalled
- 102 units
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Potential component failure in the Gradient Coil could product smoke and/or fire.
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.
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