Rhode Island Recalls

2,193 recalls on record affecting Rhode Island

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.

View recall details →

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.

View recall details →

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.

View recall details →

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.

View recall details →

medical Class II
2017-02-01

Sekisui Diagnostics P.E.I. Inc. recalls Sekisui Diagnostics Ammonia L3K¿ Assay; Catalog Number: 293-

Certain lots are showing an atypical decrease in optical density (OD) over time, which may result in an impact to performance at the high end of the linear range.

View recall details →

medical Class II
2017-02-01

Philips Electronics North America Corporation recalls Velara Generator with an old Firmware version used with Phil

System may lock up.

View recall details →

medical Class II
2017-02-01

Philips Electronics North America Corporation recalls Velara Generator with an old Firmware version used with the

System may lock up.

View recall details →

medical Class II
2017-02-15

Invacare Corporation recalls Foot Section - BAR5490IVC

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

View recall details →

Showing 20 of 2,193 recalls. Use search to filter further.