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. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2848128500 of 50,914 recalls

FoodSeptember 8, 2017· Apple King, LLC

Recalled Item: Fuji apples Recalled by Apple King, LLC Due to Fuji apples are recalled...

The Issue: Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 7, 2017· Garden Of Life, LLC

Recalled Item: Garden of Life Recalled by Garden Of Life, LLC Due to The product may pose a...

The Issue: The product may pose a choking hazard to newborns due to the thickness of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2017· Radiometer America Inc

Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...

The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex Unit Dose 15 ml Normal Saline ¿ Recalled by Medex Cardio-Pulmonary...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿ Recalled by...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿ Recalled...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Irrisept OR Recalled by Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ Recalled by...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline Prefilled 550 ml Sterile¿¿ ¿ Recalled by Medex Cardio-Pulmonary...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
FoodSeptember 5, 2017· NOW Foods

Recalled Item: Organic Coconut Sugar Recalled by NOW Foods Due to Undeclared Gluten

The Issue: Undeclared gluten found in the product and the product is labeled "Gluten Free".

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2017· Genentech, Inc.

Recalled Item: Activase (alteplase) Recalled by Genentech, Inc. Due to...

The Issue: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 5, 2017· Teva Pharmaceuticals USA

Recalled Item: Acarbose Tablets Recalled by Teva Pharmaceuticals USA Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration...

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

Class II — Potential Health HazardOngoing
Refund