Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,572 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,572 in last 12 months

Showing 1012110140 of 27,833 recalls

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 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: 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: 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
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: 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 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: 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 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: 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 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 3, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· LumiraDx

Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...

The Issue: Two lots of test strips failed QC testing using blank buffer due to false...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2021· Philips North America Llc

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...

The Issue: Manufacturing failed to follow process steps resulting in the distribution...

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

Class II — Potential Health HazardOngoing