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. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2902129040 of 50,914 recalls

Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Microline Surgical, Inc.

Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...

The Issue: The heat-shrink insulation tube may split during autoclave...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Bios S.r.l.

Recalled Item: THERMI250 Radiofrequency System. Intended to provide heating for the purpose...

The Issue: In some systems, the unit continues to emit RF energy after the PAUSE button...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2017· Pfizer Inc.

Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Halyard 24-Hour Oral Care Kit q2 Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Halyard 24-Hour Oral Care Kit q4 Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 11, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...

The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...

The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2017· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA...

The Issue: Instruments may, under certain specific circumstances listed below, fail to...

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

Class II — Potential Health HazardOngoing
FoodJuly 10, 2017· Reshmi's Group Inc.

Recalled Item: Sooji Coarse Recalled by Reshmi's Group Inc. Due to Undeclared Wheat

The Issue: Undeclared wheat. Sooji Coarse is recalled because product contains Semolina...

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

Class II — Potential Health HazardOngoing
Refund