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. 2,438 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,438 in last 12 months

Showing 3666136680 of 50,914 recalls

DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Rocuronium Bromide 50 MG/5ML INJ. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Lorazepam 2 mg/mL Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 11, 2015· ConvaTec, Inc

Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...

The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
DrugNovember 10, 2015· Northwind Pharmaceuticals LLC

Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...

The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa Colostrum Capsules Recalled by Immuno - Dynamics, Inc Due to The...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa 1 Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand and...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Lozenges Recalled by Immuno - Dynamics, Inc Due to The PerCoBa...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund