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. 2,517 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,517 in last 12 months

Showing 1000110020 of 27,456 recalls

Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Meridian Bioscience Inc

Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...

The Issue: Use of the kits after incorrect storage could lead to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Mizuho OSI

Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...

The Issue: There is a potential that hand control units may cause the tabletop to slide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· OraSure Technologies, Inc.

Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...

The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack CP 1/4-1/4 Pediatric Set 1/B (PERFUSION M484901D...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK HY10J00R6 ECC SMALL CAR). The Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Perfusion Pack (CUSTOM PACK HY11B40R1 1/4 RESPIRATO). The...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing