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GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc Recalls

All product recalls associated with GE OEC Medical Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 24261–24280 of 25000 recalls

GE OEC Medical Systems, Inc: ENTrak Plus Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

Allen Medical Systems One Post Office Square: Neuro Adapter 2 used with the Berchtold B-810 Surgical Ta...

Neuro adapter may fail to engage and adequately clamp to the surgical table, resulting in movement

FDAJul 12, 2004SC• Allen Medical Systems One Post Office Square

Arch Swing (Playworld Systems) – Structural Weakness (2004)

The 2-3/8" Arch Swing Model # 0289 and the 2-3/8" Arch Swing Add-A-Bay Model # 0380 have arched metal side supports and a welded top rail that supports two swings. The swing sets are made from 2-3/8" steel tubing and come in a variety of solid colors.

1...1212 121312141215 1216...1250

Page 1214 of 1250Next

Jul 12, 2004

Nationwide

• Playworld Systems Inc., of Lewisburg, Pa.

GE OEC Medical Systems, Inc: ENTrak Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

MDS Canada Inc. DBA MDS Nordion: Theratron Phoenix Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron 780C Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron 1000E Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron 780E Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron Elite 100 Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron 1000 Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

MDS Canada Inc. DBA MDS Nordion: Theratron Elite 80 Cobalt Radiotherapy

The source locking device may not fit properly through the smaller opening in the new field light shield which could prevent the source from being returned manually under emergency conditions.

FDAJul 8, 2004FL, IN, KS• MDS Canada Inc. DBA MDS Nordion

Roche Molecular Systems Inc: Amplicor [3] AV-HRP. (Avidin-HRP (Horseradish Peroxidase...

An increased frequency of 'blue foci' that potentially can cause elevated A450 background in microwell plate wells after the addition of conjugate reagent during PCR detection.

FDAJul 7, 2004CT, IN• Roche Molecular Systems Inc

Terumo Cardiovascular Systems Corp: Sarns brand Retrograde Cardioplegia Cannulae, manual -inf...

The product is labeled as sterile, but sterility is compromised because some of the packages were not sealed.

FDAJul 7, 2004Nationwide• Terumo Cardiovascular Systems Corp

B. Braun Medical, Inc.: Standard and Custom Spinal Trays with 5% Lidocaine Hydroc...

drug ampuls in kits contain particulates

FDAJul 6, 2004Nationwide• B. Braun Medical, Inc.

Multi-Surface Steam Cleaner (Euroflex) – Performance Issue (2004)

Euroflex Monster 55 – 1600-Watt Multi-surface Steam Cleaner with Attachments. The steam cleaner has a red body and black cords and attachments. The word "monster" is written on the side of the steam cleaner.

CPSCJul 6, 2004Nationwide• Euroflex Americas Inc., of New York, N.Y.

Hunting Tree Stands (Rivers Edge) – Safety Risk (2004)

The recalled Big Foot and Lite Foot Series hunting tree stands are "hang-on" stands that can be identified by a yellow warning label affixed to the stand that reads: "Rivers Edge Hunting Products." These tree stands have dual post seat uprights and a gold-colored strap hook bracket. Only these model tree stands with the gold-colored bracket are included in this recall.

CPSCJul 6, 2004Nationwide• Rivers Edge/Ardisam, Inc., of Cumberland, Wis.

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000 Roller Pump; Model 9000; Cat...

Roller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 115V; Model 800...

Roller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Fisher Diagnostic, A Company of Fisher Scientific LLC: Pacific Hemostasis D-Dimer Assay Kit, Fisher Diagnostics ...

Defective reagent may cause in vitro diagnostic test kit to yield false positive test results in clinical samples.

FDAJul 1, 2004Nationwide• Fisher Diagnostic, A Company of Fisher Scientific LLC

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 1040V; Model 80...

Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp