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. 2,646 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,646 in last 12 months

Showing 70217040 of 50,914 recalls

Medical DeviceDecember 18, 2023· Vortex Surgical Inc.

Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...

The Issue: Reason for the voluntary recall is residue was identified on the two forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2023· St. Jude Medical, Atrial Fibrillation Division, Inc.

Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...

The Issue: When the catheters are used with the EnSiteX EP System, the system does not...

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

Class II — Potential Health HazardOngoing
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies)...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Chocolate Chili Coconut (12...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Brown Butter Snickerdoodle (12...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 15, 2023· Eban's Bakehouse LLC

Recalled Item: Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies)...

The Issue: Undeclared Allergens - Milk and Soy

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2023· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 15, 2023· Olympus Corporation of the Americas

Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...

The Issue: The jaw may fracture prior to the procedure during the inspection instructed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Globus Medical, Inc.

Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...

The Issue: Devices may not be rendered sterile due to an internal gap that may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...

The Issue: Potential for a negative bias with quality control (QC) and patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Hologic, Inc.

Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...

The Issue: Due to potential false positive Flu B results when a sample was also...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...

The Issue: Their is a potential for false positive results when using Pneumonia panel.

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

Class II — Potential Health HazardOngoing