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. 2,646 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,646 in last 12 months

Showing 65216540 of 28,488 recalls

Medical DeviceApril 25, 2023· Linkbio Corp.

Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....

The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 2.5in Cath Recalled by Avanos Medical, Inc....

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Abbott Ireland Limited

Recalled Item: Alinity i Anti-TPO Reagent Kit Recalled by Abbott Ireland Limited Due to Due...

The Issue: Due to a manufacturing fill volume error, Alinity i Anti-TPO Reagent...

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

Class III — Low RiskOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Kit Basic Filter Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: ambIT Cassette Filter Male Luer Recalled by Avanos Medical, Inc. Due to Some...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 5in Cath Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing