Recall Register

Device recall: Achieva 1.5T, Magnetic Resonance System.

Class II FDA enforcement event 94233. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Patient support table floor plate may be incorrectly installed.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Philips North America Llc started this device recall on 12 Mar 2024. The firm address in the FDA record is in Cambridge, MA. FDA put the recall in Class II. FDA event 94233 has 41 product records. The first FDA enforcement report date is 24 Apr 2024. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia,…

Recalling firm

Philips North America Llc, Cambridge, MA.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

41 product records in the event.

FDA event 94233: product records
Recall numberProductQuantityClassStatusReport date
Z-1550-2024Achieva 1.5T, Magnetic Resonance System.1,921 unitsClass IIOngoing24 Apr 2024
Z-1551-2024Achieva 1.5T Conversion, Magnetic Resonance System.115 unitsClass IIOngoing24 Apr 2024
Z-1552-2024Achieva 1.5T Initial, Magnetic Resonance System.69 unitsClass IIOngoing24 Apr 2024
Z-1553-2024Achieva 3.0T, Magnetic Resonance System.511 unitsClass IIOngoing24 Apr 2024
Z-1554-2024Achieva 3.0T for PET, Magnetic Resonance System.1 unitClass IIOngoing24 Apr 2024
Z-1555-2024Achieva 3.0TX for PET, Magnetic Resonance System.1 unitClass IIOngoing24 Apr 2024
Z-1556-2024Achieva XR, Magnetic Resonance System.49 unitsClass IIOngoing24 Apr 2024
Z-1557-2024Enterprise 1.5T, Magnetic Resonance System.33 unitsClass IIOngoing24 Apr 2024
Z-1558-2024Evolution Upgrade 3.0T, Magnetic Resonance System.1 unitClass IIOngoing24 Apr 2024
Z-1559-2024GYROSCAN ACS-NT, Magnetic Resonance System.50 unitsClass IIOngoing24 Apr 2024
Z-1560-2024GYROSCAN T10-NT, Magnetic Resonance System.40 unitsClass IIOngoing24 Apr 2024
Z-1561-2024GYROSCAN T5, Magnetic Resonance System.7 unitsClass IIOngoing24 Apr 2024
Z-1562-2024GYROSCAN T5-NT, Magnetic Resonance System.23 unitsClass IIOngoing24 Apr 2024
Z-1563-2024Ingenia 1.5T, Magnetic Resonance System.2,242 unitsClass IIOngoing24 Apr 2024
Z-1564-2024Ingenia 1.5T CX, Magnetic Resonance System.143 unitsClass IIOngoing24 Apr 2024
Z-1565-2024Ingenia 1.5T S, Magnetic Resonance System.135 unitsClass IIOngoing24 Apr 2024
Z-1566-2024Ingenia 3.0T, Magnetic Resonance System.1,509 unitsClass IIOngoing24 Apr 2024
Z-1567-2024Ingenia 3.0T CX, Magnetic Resonance System.342 unitsClass IIOngoing24 Apr 2024
Z-1568-2024Ingenia Ambition S, Magnetic Resonance System.344 unitsClass IIOngoing24 Apr 2024
Z-1569-2024Ingenia Ambition X, Magnetic Resonance System.404 unitsClass IIOngoing24 Apr 2024
Z-1570-2024Ingenia Elition S, Magnetic Resonance System.131 unitsClass IIOngoing24 Apr 2024
Z-1571-2024Ingenia Elition X, Magnetic Resonance System.448 unitsClass IIOngoing24 Apr 2024
Z-1572-2024Intera 0.5T Standard, Magnetic Resonance System.14 unitsClass IIOngoing24 Apr 2024
Z-1573-2024Intera 1.0T Omni/Stellar, Magnetic Resonance System.27 unitsClass IIOngoing24 Apr 2024
Z-1574-2024Intera 1.0T Power/Pulsar, Magnetic Resonance System.19 unitsClass IIOngoing24 Apr 2024
Z-1575-2024Intera 1.5T, Magnetic Resonance System.347 unitsClass IIOngoing24 Apr 2024
Z-1576-2024Intera 1.5T Achieva IT Nova, Magnetic Resonance System.2 unitsClass IIOngoing24 Apr 2024
Z-1577-2024Intera 1.5T Achieva Nova, Magnetic Resonance System.46 unitsClass IIOngoing24 Apr 2024
Z-1578-2024Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.20 unitsClass IIOngoing24 Apr 2024
Z-1579-2024Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.12 unitsClass IIOngoing24 Apr 2024
Z-1580-2024Intera 1.5T Master/Nova, Magnetic Resonance System.107 unitsClass IIOngoing24 Apr 2024
Z-1581-2024Intera 1.5T Omni/Stellar, Magnetic Resonance System.22 unitsClass IIOngoing24 Apr 2024
Z-1582-2024Intera 1.5T Power/Pulsar, Magnetic Resonance System.115 unitsClass IIOngoing24 Apr 2024
Z-1583-2024Intera 1.5T R11, Magnetic Resonance System.25 unitsClass IIOngoing24 Apr 2024
Z-1584-2024Intera 3.0T Quasar Dual, Magnetic Resonance System.9 unitsClass IIOngoing24 Apr 2024
Z-1585-2024Intera Achieva 1.5T Pulsar, Magnetic Resonance System.24 unitsClass IIOngoing24 Apr 2024
Z-1586-2024Intera CV, Magnetic Resonance System.8 unitsClass IIOngoing24 Apr 2024
Z-1587-2024MR 5300, Magnetic Resonance System.166 unitsClass IIOngoing24 Apr 2024
Z-1588-2024MR 7700, Magnetic Resonance System.26 unitsClass IIOngoing24 Apr 2024
Z-1589-2024SmartPath to dStream for 1.5T, Magnetic Resonance System.672 unitsClass IIOngoing24 Apr 2024
Z-1590-2024SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.41 unitsClass IIOngoing24 Apr 2024

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2024
970
Share of these events in Class II
87%
Product records in this event
41Median of the firm: 1
Events of the firm on the register
129

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 94233. https://recallregister.com/fda/ii/94233/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia,…
What quantity of product is in FDA event 94233?
The event has 41 product records. The first record gives this quantity: 1,921 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2024 have the same class?
87% of the 970 device events that started in 2024 are in Class II.