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. 2,567 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,567 in last 12 months

Showing 1646116480 of 50,914 recalls

Medical DeviceMarch 3, 2021· CareFusion 303, Inc.

Recalled Item: BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad Recalled by...

The Issue: Pump Module keypad lifting, and Fluid ingress could result in 1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 3, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console Recalled by...

The Issue: An electrical component within the system controller module of certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 3, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information...

The Issue: Patient related messages created in RayCare 3B, RayCare 4A will be lost when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed...

The Issue: SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2021· A-S Medication Solutions LLC.

Recalled Item: Acetaminophen Recalled by A-S Medication Solutions LLC. Due to Labeling:...

The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 2, 2021· Ferring Pharmaceuticals Inc

Recalled Item: Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH...

The Issue: Failed pH specifications: Out of Specification pH results for 0.9% Sodium...

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

Class III — Low RiskOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Wilton Valentine Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Wilton Autumn Assorted Treat Toppings Sprinkles Recalled by Wilton...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Holiday Home Assorted Treat Toppings Recalled by Wilton Industries Inc Due...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 2, 2021· Wilton Industries Inc

Recalled Item: Wilton Holiday Mix Sprinkles Recalled by Wilton Industries Inc Due to...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 2, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: BCS XP System: Multipurpose system for in vitro coagulation studies....

The Issue: Siemens Healthcare Diagnostics Products GmbH has confirmed that the BCS XP...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2021· AZURE BIOTECH INC

Recalled Item: Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Recalled by...

The Issue: Due to Products being incorrect labeling "for diagnostic use" and labelled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2021· Terumo Cardiovascular Systems Corporation

Recalled Item: Consist of a distal connection mechanism (either standard Terumo Ball...

The Issue: There is a potential for the stainless steel locking plates on the device's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2021· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS - Radiological Image Processing System - Product Usage:...

The Issue: The wrong patient information may be displayed in the viewer or PowerJacket.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2021· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...

The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2021· Cellex

Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...

The Issue: The kit does not have an emergency use authorization (EUA).

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2021· James Leckey Design Ltd

Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...

The Issue: Due to a failure of the welds, the casters detached from the rear legs of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2021· Hitachi Medical Systems America Inc

Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...

The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...

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

Class II — Potential Health HazardOngoing