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 1882118840 of 50,914 recalls

Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2020· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...

The Issue: Presence of Particulate Matter: confirmed customer complaint for the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 8, 2020· K F K Seasonings Llc

Recalled Item: Organic Chipotle Chile Ground Recalled by K F K Seasonings Llc Due to...

The Issue: Undeclared tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 8, 2020· K F K Seasonings Llc

Recalled Item: Organic Ground Oregano Recalled by K F K Seasonings Llc Due to Undeclared Tree

The Issue: Undeclared tree nuts and Crustacea.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 8, 2020· K F K Seasonings Llc

Recalled Item: Chili Powder Recalled by K F K Seasonings Llc Due to Undeclared Tree

The Issue: Undeclared tree nuts and Crustacea.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 8, 2020· Ge Healthcare

Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...

The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2020· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...

The Issue: An error in the calculation of the Michigan Ranges can generate an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If an examination is interrupted when the InSpect Projection View (PV) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker 1 End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing