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 10411060 of 50,914 recalls

DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone 87.5 MG Recalled by FARMAKEIO OUTSOURCING LLC Due to CGMP...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 14, 2025· Beckman Coulter Ireland, Inc.

Recalled Item: BECKMAN COULTER BICARBONATE OSR6237 OSR6637 OSR6x37 Bicarbonate is Recalled...

The Issue: Bicarbonate reagent may generate falsely high Bicarbonate results due to...

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

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

Recalled Item: Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V...

The Issue: Continued reports of positive cultures and infections have identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2025· Becton Dickinson & Company

Recalled Item: BD Luer Tip Caps Recalled by Becton Dickinson & Company Due to BD has...

The Issue: BD has confirmed through internal testing that certain device trays failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· MRIMed Inc.

Recalled Item: MRI LED Mobile Exam Light Battery This non-magnetic Recalled by MRIMed Inc....

The Issue: Due to battery component overheating while charging resulting in melting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· Paragon 28, Inc.

Recalled Item: Phantom Fibula Nail Recalled by Paragon 28, Inc. Due to Fibula nail system...

The Issue: Fibula nail system intended for use in fixation of fibular fractures and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· TMJ Solutions Inc

Recalled Item: TMJ Bilateral Implant Sterile EO Recalled by TMJ Solutions Inc Due to...

The Issue: Patient-fitted temporomandibular joint implant contained discrepancy in...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 7.5mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 2.5 mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· QuVa Pharma, Inc.

Recalled Item: R.E.C.K. (Ropivacaine HCl Recalled by QuVa Pharma, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 10 mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Lannett Company Inc.

Recalled Item: Niacin Extended-release Tablets Recalled by Lannett Company Inc. Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2025· Thoratec LLC

Recalled Item: CentriMag Blood Pump Recalled by Thoratec LLC Due to Acute circulatory...

The Issue: Acute circulatory support system pump may not fit into the motor and reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing