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. 2,665 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,665 in last 12 months

Showing 39613980 of 50,914 recalls

DrugOctober 30, 2024· Baxter Healthcare Corporation

Recalled Item: Regadenoson Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Labeling: Missing Label

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2024· INCIPIO DEVICES

Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...

The Issue: Recalled lot does not meet specification and has reported incidents of...

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

Class II — Potential Health HazardOngoing
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: La Bonne Vie Camembert 8oz Recalled by SAVENCIA CHEESE USA Due to Potential...

The Issue: potential to be contaminated with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: Aldi Emporium Selection Brie 8oz Recalled by SAVENCIA CHEESE USA Due to...

The Issue: potential to be contaminated with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: Glenview Farms Spreadable Brie 2 Recalled by SAVENCIA CHEESE USA Due to...

The Issue: potential to be contaminated with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Tablet/Capsule Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2024· VIONA PHARMACEUTICALS INC

Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...

The Issue: Due to manufacturing defects observed on Locking Caps that affect the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...

The Issue: Due to manufacturing defects observed on Locking Caps that affect the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2024· Smith & Nephew Inc.

Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....

The Issue: Sterile barrier breach due to inadequate packaging design that could not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Boston Scientific Corporation

Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...

The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Boston Scientific Corporation

Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...

The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...

The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...

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

Class III — Low RiskOngoing
FoodOctober 25, 2024· Grand Central Bakery FRE Co Inc

Recalled Item: U-BAKE Pie Crust (Pastry Round) Recalled by Grand Central Bakery FRE Co Inc...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 25, 2024· Grand Central Bakery FRE Co Inc

Recalled Item: U-BAKE Chicken Pot Pie Recalled by Grand Central Bakery FRE Co Inc Due to...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 25, 2024· Grand Central Bakery FRE Co Inc

Recalled Item: U-BAKE Marionberry Pie Recalled by Grand Central Bakery FRE Co Inc Due to...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund