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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96999

9 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 29, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Philips North America

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

9 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 9

Achieva XR Product Numbers: (1) 781153, (2) 781253;

Z-1928-2025
Recall number
Z-1928-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
6 units (5 US, 1 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Numbers: (1) 781153, (2) 781253; UDI-DI: (1) no UDI, (2) no UDI; Serial Numbers: All serial numbers;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 2 of 9

Intera 1.5T Achieva IT Nova Product Number: 781175

Z-1929-2025
Recall number
Z-1929-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781175; UDI-DI: no UDI; Serial Number: 15003;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 3 of 9

Intera 1.5T Achieva Nova Product Number: 781172;

Z-1930-2025
Recall number
Z-1930-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
16 units (1 US, 15 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781172; UDI-DI: no UDI; Serial Numbers: 21218, 21217, 21216, 21289, 21349, 12146, 12063, 12086, 20069, 21027, 21198, 12099, 18641, 21476, 18623, 12078;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 4 of 9

Intera 1.5T Achieva Nova-Dual Product Number: 781173;

Z-1931-2025
Recall number
Z-1931-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
3 units (1 US, 2 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781173; UDI-DI: no UDI; Serial Numbers: 13010, 13006, 21501;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 5 of 9

Intera 1.5T Explorer/Nova Dual Product Number: 781108;

Z-1932-2025
Recall number
Z-1932-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
1 unit (OUS only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781108; UDI-DI: no UDI; Serial Number: 9025;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 6 of 9

Intera 1.5T Master/Nova Product Number: 781106;

Z-1933-2025
Recall number
Z-1933-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
2 units (US only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781106; UDI-DI: no UDI; Serial Numbers: 8009, 18863;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 7 of 9

Intera 1.5T Omni/Stellar; Product Number: 781104;

Z-1934-2025
Recall number
Z-1934-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
2 units (OUS only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781104; UDI-DI: no UDI; Serial Numbers: 10403, 18969;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 8 of 9

Intera Achieva 1.5T Pulsar; Product Number: 781171;

Z-1935-2025
Recall number
Z-1935-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
4 units (1 US, 3 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 781171; UDI-DI: no UDI; Serial Numbers: 11044, 11039, 18627, 11069;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

device · product 9 of 9

SmartPath to dStream for 1.5T¿; Product Number: 782146;

Z-1936-2025
Recall number
Z-1936-2025
Initiated
May 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

Code information

Product Number: 782146; UDI-DI: no UDI; Serial Number: 13013;

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya, Mexico, Poland, Portugal, Spain.

Field note

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