Minnesota Recalls

5,380 recalls on record affecting Minnesota

medical Class II
2017-01-04

GE Healthcare, LLC recalls Prestige II

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

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medical Class II
2017-01-04

GE Healthcare, LLC recalls SFX

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls ADVANTX LCN+

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls ADVANTX LCLP+

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Legacy

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Innova 2000

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Prestilix

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls ADVANTX LCV+

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls RFX

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Prestige SI

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls ADVANTX LCA

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Precision 500D

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-04

GE Healthcare, LLC recalls Prestige VH

GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.

View recall details →
medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls The OEC 9900 Elite mobile fluoroscopy system is designed to

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

Stryker Sustainability Solutions recalls Reprocessed Electrophysiology Catheter Cables Catalog Numbe

A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.

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medical Class II
2017-01-18

Stryker Sustainability Solutions recalls Reprocessed Ablation Catheter Cable Catalog Number: CR3425C

A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 680

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is des

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-25

Elekta, Inc. recalls Monaco RTP System. Used to make treatment plans for patie

Incorrect dose after editing beam number an wedge angle.

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medical Class II
2017-01-25

DICOM GRID INC recalls Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R S

A software error caused the window/level to become the same in one series regardless if the image had different levels; image results have a washed-out grey appearance.

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Showing 20 of 5,380 recalls. Use search to filter further.