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 701720 of 28,488 recalls

Medical DeviceOctober 18, 2025· Auris Health, Inc

Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...

The Issue: Potential that product was leak tested with equipment outside of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Straumann USA LLC

Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...

The Issue: The possibility for this product that is intended for demonstration purposes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· INTELERAD MEDICAL SYSTEMS INCORPORATED

Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...

The Issue: Software application that receives digital images and data to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...

The Issue: If infusion pump is dropped or severely jarred this may damage the pump...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an Recalled...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model Number: SR103B. Intended for use as an Recalled by...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2025· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed...

The Issue: Due to an issue (potential breakage) with the shaft for the mounting of the...

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

Class II — Potential Health HazardOngoing
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
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