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 3186131880 of 50,914 recalls

Medical DeviceDecember 21, 2016· PerkinElmer Health Sciences, Inc.

Recalled Item: AutoDELFIA¿ Plate Processor Recalled by PerkinElmer Health Sciences, Inc....

The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures

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

Class III — Low RiskOngoing
Medical DeviceDecember 21, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: Used to make treatment plans Recalled by...

The Issue: Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 2008K2 Series : Hemodialysis System Recalled by Fresenius Medical...

The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 2008T Series Hemodialysis System Recalled by Fresenius Medical...

The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...

The Issue: Negative bias results with the IMMULITE¿ /IMMULITE¿ 1000 Third Generation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Becton Dickinson & Company

Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...

The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...

The Issue: There is a potential for biased results to be generated over the 10 day...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...

The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2016· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: iOS and Android: Under certain conditions the affected app versions may...

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

Class II — Potential Health HazardOngoing
FoodDecember 20, 2016· Hungry Heart Bakery

Recalled Item: Cracker Jax Recalled by Hungry Heart Bakery Due to Cracker Jax are recalled...

The Issue: Cracker Jax are recalled because butter is declared, but milk is not...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Hungry Heart Bakery

Recalled Item: Chocolate Chip Sea Salt Cookies Recalled by Hungry Heart Bakery Due to...

The Issue: Chocolate Chip Sea Salt Cookies are recalled due to undeclared wheat and soy...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Herr Foods, Inc.

Recalled Item: Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 oz and 8.0 oz...

The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Hungry Heart Bakery

Recalled Item: Walnut Chocolate Chunk Cookies Recalled by Hungry Heart Bakery Due to...

The Issue: Walnut Chocolate Chunk Cookies are recalled due to undeclared wheat and soy...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Herr Foods, Inc.

Recalled Item: Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.0 oz. Recalled by...

The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Hungry Heart Bakery

Recalled Item: Peanut Butter Cookies Recalled by Hungry Heart Bakery Due to Undeclared Soy

The Issue: Peanut Butter Cookies are recalled due to undeclared soy (from the pan...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Accord Healthcare, Inc.

Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...

The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class III — Low RiskOngoing
Refund