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. 2,681 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,681 in last 12 months

Showing 17011720 of 50,914 recalls

Medical DeviceAugust 6, 2025· Olympus Corporation of the Americas

Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....

The Issue: Potential for undetected, deformed a-traumatic tips.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to...

The Issue: Inserter, used as part of a system with an intervertebral body fusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
FoodAugust 5, 2025· M.O.M Enterprises, LLC.

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

The Issue: Potential for spoilage due to yeast contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2025· Haleon US Holdings LLC

Recalled Item: Sensodyne PRONAMEL (Potassium nitrate 5% Recalled by Haleon US Holdings LLC...

The Issue: Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is...

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Spironolactone Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Presence of foreign substance: identified as aluminum.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Tandem Diabetes Care, Inc.

Recalled Item: t:slim X2 insulin pump with Interoperable Technology Recalled by Tandem...

The Issue: A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle Radiation Therapy Planning System: Multimodality Simulation...

The Issue: Due to a software issue, there is a potential image error of the Region of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number:...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Recalled by Integra...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing