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. 2,557 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,557 in last 12 months

Showing 1870118720 of 50,914 recalls

Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis PLUS 6 Fr Catheter Drainage Tray Recalled by Carefusion 2200...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc Due...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T 5 Fr Thora-Para Tray With 5 Fr. Catheter and Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T 8 Fr Thora-Para Tray With 8 Fr. Catheter and Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
DrugMay 27, 2020· Pfizer Inc.

Recalled Item: Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg Recalled by...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 27, 2020· Apotex Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Apotex Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...

The Issue: Failed Impurities/Degradation Specifications: potential migration of...

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

Class III — Low RiskOngoing
Refund