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. 1,730 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,730 in last 12 months

Showing 4800148020 of 50,914 recalls

FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Arnold Healthfull 45 Calories Per Slice Multigrain Bread Recalled by Bimbo...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Blue Planet Foods, Inc.

Recalled Item: Hannaford Autumn Spice Granola Recalled by Blue Planet Foods, Inc. Due to...

The Issue: Blue Planet products that contain the two recalled Dakota Specialty Milling...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Blue Planet Foods, Inc.

Recalled Item: Heartland Recalled by Blue Planet Foods, Inc. Due to Blue Planet products...

The Issue: Blue Planet products that contain the two recalled Dakota Specialty Milling...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2013· Hospira Inc.

Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...

The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...

The Issue: It was reported from a complaint that study category labels of "Prior" and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...

The Issue: A software defect was discovered that causes images to be out of context...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product is being recall due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Jevantique (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Dr Reddys Laboratories Tennessee LLC

Recalled Item: Amoxicillin for Oral Suspension Recalled by Dr Reddys Laboratories Tennessee...

The Issue: Microbial Contamination of Non-Sterile Products: Suspensions made from these...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Hospira Inc.

Recalled Item: METRONIDazole Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance...

The Issue: This field change order is being released to update software and customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...

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

Class III — Low RiskOngoing