CLASS II Device recall · Reported 6 Mar 2019 · FDA Enforcement Report

SmartPath to dStream for 1.5T recalled by Philips Medical Systems

Philips Medical Systems Nederlands is recalling SmartPath to dStream for 1.5T, distributed nationwide in the US. The recall was initiated on 21 Dec 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll systems
Quantity recalled11226 total

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0900-2019
FDA event ID
82038
Classification
Class II
Status
Terminated
Recall initiated
21 Dec 2018
FDA classified
22 Feb 2019
Reported
6 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

21 Dec 2018Recall initiated by company
22 Feb 2019Classified by FDA+63 days
6 Mar 2019Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.

Product as listed by the FDA

SmartPath to dStream for 1.5T, Model Number 781260. Nuclear Magnetic Resonance Imaging System

Where it was distributed

U.S. Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.

Which lots are affected?

All systems

Where was it sold?

U.S. Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

63 other products · FDA event 82038

This product is part of a recall event; the main page for the event is Achieva XR 1.5T/3.0T recalled by Philips Medical Systems.

ReportedClassRecallCompanyReasonWhere
CLASS IIAchieva XR 1.5T/3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IISmartPath to dStream for XR and 3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T Achieva CV Nova recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIEnterprise 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.0T Power/Pulsar recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia Elition X recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMR RT recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera Achieva 1.5T Nova recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T Conversion recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T Explorer/Nova Dual recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMultiva 1.5T 8 R5 (ZBO) recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera Achieva 1.5T Nova Dual recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T TX recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMultiva 1.5T 8 R5 recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera Achieva 1.5T Pulsar recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMultiva 1.5T 16 R5 (ZBO) recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 1.5T CX (ZBO) recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T R11 recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T X-series recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 7.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T Omni/Stellar recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 1.5T S recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMarlin 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMr-or 3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IINZM101 Ingenia 1.5T Linac recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T X recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T Power/Pulsar recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T CV recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 3.0T CX recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 1.5T CX recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMultiva 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMultiva 1.5T 16 R5 recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.0T Omni/Stellar recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T High Performance recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 3.0T Master/Quasar Dual recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIProdiva CS recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T TX for PET recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIPanorama 1.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T Master/Nova recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera Achieva 1.5T IT Nova Dual recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia 3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T TX-series recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T Conversion recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera IT recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIProdiva CX recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva XR 1.5T/3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera Achieva 1.5T IT Nova recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia Ambition X recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia Elition S recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIngenia Ambition S recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIMr-or 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 3.0T for PET recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIPanorama 1.0T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 0.5T Standard recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIAchieva 1.5T recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide
CLASS IIIntera 1.5T High Performance recalled by Philips Medical SystemsPhilips Medical Systems NederlandsOtherNationwide

More recalls from Philips Medical Systems Nederlands

All 79

Other Imaging Equipment recalls

All 2,336