New York Recalls

8,788 recalls on record affecting New York

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

Siemens Medical Solutions USA, Inc recalls SOMATOM Scope, Computed tomography x-ray system

Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.

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medical Class II
2017-01-04

Siemens Medical Solutions USA, Inc recalls SOMATOM Scope Power, Computed tomography x-ray system

Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.

View recall details →

medical Class II
2017-01-04

Shimadzu Medical Systems recalls Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

Shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION due to possibility of oil leaking from the x-ray tube housing under certain conditions.

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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

Siemens Medical Solutions USA, Inc recalls SOMATOM Perspective, Computed tomography x-ray system

Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective 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
2017-01-11

Boston Scientific Corporation recalls Boston Scientific, INGEVITY" MRI Leads, Sterile EO, RxOnly.

Boston Scientific is conducting a recall on Boston Scientific INGEVITY" MRI endocardial pacing leads. There is a possibility that the polyurethane boot at the terminal end of the lead was not securely connected to the lead body.

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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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Showing 20 of 8,788 recalls. Use search to filter further.