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 681700 of 50,914 recalls

Medical DeviceNovember 17, 2025· Sheathing Technologies Inc

Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...

The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Orthofix NorthStar OCT Navigation Surgical Technique Guide Recalled by...

The Issue: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly...

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

Class II — Potential Health HazardOngoing
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted Recalled by...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Green Tea Flavor bright lime green packaging Recalled by Prime...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Software version 5.10.1 and earlier contain anomalies that have the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 13, 2025· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...

The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...

The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
FoodNovember 12, 2025· Genepro Protein, Inc.

Recalled Item: Genepro Whey 4th Generation Plasma Treated Protein Recalled by Genepro...

The Issue: Product is mislabeled - the labeling contains incorrect ingredient...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 12, 2025· Medical Products Laboratories, Inc.

Recalled Item: Walgreens Saline Nasal Spray WITH XYLITOL Recalled by Medical Products...

The Issue: Microbial contamination of a non-sterile product - microorganism found to be...

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

Class II — Potential Health HazardOngoing
Refund