Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,562 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,562 in last 12 months

Showing 1684116860 of 28,488 recalls

Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT VDD SL Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Intel-GE Care Innovations LLC

Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...

The Issue: It was discovered that in certain situations, including partial sessions and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Reliance Medical Products Inc

Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...

The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Cellavision AB

Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...

The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...

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

Class II — Potential Health HazardOngoing