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. 2,401 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,401 in last 12 months

Showing 1822118240 of 27,456 recalls

Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Pride Mobility Products Corp

Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...

The Issue: The interface between the TB3 back and tilt base can separate when tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Merit Medical Systems, Inc.

Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...

The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing