Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2670126720 of 27,456 recalls

Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE 3 Blood and Fluid Warmer Recalled by Smiths Medical...

The Issue: HOTLINE 3 Blood and Fluid Warmer( Reorder No. HL-390 ) disposable is not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Bridgepoint Medical

Recalled Item: BridgePoint Medical Recalled by Bridgepoint Medical Due to BridgePoint...

The Issue: BridgePoint Medical Inc. is voluntarily recalling Stingray Catheter, Model...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Sunrise Medical (US) LLC

Recalled Item: Padded Swing Away Arm Rest with Receiver Recalled by Sunrise Medical (US)...

The Issue: Reports of injury when the Padded Swing Away Armrest is used for full body...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V. The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing