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. 1,155 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,155 in last 12 months

Showing 1321–1340 of 50,914 recalls

Medical DeviceSeptember 15, 2025· Alcon Research LLC

Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2025· Argon Medical Devices, Inc

Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...

The Issue: Due to complaints of increased resistance when advancing the dilator within...

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

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2025· M.O.M Enterprises, LLC.

Recalled Item: Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Due to...

The Issue: Potential yeast contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2025· Diagnostica Stago, Inc.

Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...

The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: TENACIO Pump with InhibiZone Recalled by Boston Scientific Corporation Due...

The Issue: The potential for devices to experience inflation and/or deflation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing