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. 2,567 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,567 in last 12 months

Showing 1656116580 of 50,914 recalls

DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Toposar (etoposide injection USP) Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2021· Howmedica Osteonics Corp.

Recalled Item: Prosthesis Recalled by Howmedica Osteonics Corp. Due to Stryker has...

The Issue: Stryker has discovered that the internal profile of the Triathlon Tritanium...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· In2Bones, SAS

Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...

The Issue: This Field Action is being conducted following identification of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Meridian Bioscience Inc

Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...

The Issue: Use of the kits after incorrect storage could lead to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Mizuho OSI

Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...

The Issue: There is a potential that hand control units may cause the tabletop to slide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

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 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 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

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
DrugFebruary 5, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Injection 40mg/vial For I.V. infusion only...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund