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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97647

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

Open FDA event record

Event summary

Timeline bucket
September 12, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

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

14 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 14

Elscint Cardial; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0290-2026
Recall number
Z-0290-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
11 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 2 of 14

Elscint Model 4XX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0291-2026
Recall number
Z-0291-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
64 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 3 of 14

Elscint SPX4; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0292-2026
Recall number
Z-0292-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
45 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 4 of 14

Elscint SPX6; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0293-2026
Recall number
Z-0293-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
28 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 5 of 14

Elscint Varicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0294-2026
Recall number
Z-0294-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
15 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 6 of 14

Elscint Helix; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0295-2026
Recall number
Z-0295-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
3 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 7 of 14

Maxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0296-2026
Recall number
Z-0296-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
37 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 8 of 14

Millenium MG/MC; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0297-2026
Recall number
Z-0297-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
1386 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 9 of 14

Millenium Myosight; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0298-2026
Recall number
Z-0298-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
82 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 10 of 14

Millenium MPR; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0299-2026
Recall number
Z-0299-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
292 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 11 of 14

Millenium MPS; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0300-2026
Recall number
Z-0300-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
54 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 12 of 14

Optima NX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0301-2026
Recall number
Z-0301-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 13 of 14

Sopha Medical Vision (SMV) DSXi/DST-XLi,/ DST-XL/ DSTi; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0302-2026
Recall number
Z-0302-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
205 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide

device · product 14 of 14

Starcam/Camstar; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging

Z-0303-2026
Recall number
Z-0303-2026
Initiated
September 12, 2025
Classification
Class II
Status
Ongoing
Quantity
102 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Package design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Code information

all serial numbers in distribution

Distribution pattern

Worldwide