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 3184131860 of 50,914 recalls

Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The intended use listed in the English and localized language IFUs for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Elekta, Inc.

Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...

The Issue: Cross profile for Varian 60 degree wedge shows "horns."

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...

The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
FoodDecember 22, 2016· Schreiber Food International

Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....

The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 22, 2016· AGFA Healthcare Corp.

Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...

The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Mako Surgical Corporation

Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...

The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Tosoh Smd Inc

Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...

The Issue: Power outages causes reporting software to shutdown.

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

Class II — Potential Health HazardOngoing
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Jon Donaire Ice Cream Layer Cake Recalled by Rich Products Corp Due to...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CAKE Recalled by...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: RICH'S 1/4 Sheet White Cake with Vanilla Ice Cream Cake Recalled by Rich...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Jon Donaire Ice Cream Layer Cake Recalled by Rich Products Corp Due to...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

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

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

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

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2016· PerkinElmer Health Sciences, Inc.

Recalled Item: Program Update Package AutoDELFIA¿ 3.0 Recalled by PerkinElmer Health...

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· PerkinElmer Health Sciences, Inc.

Recalled Item: DELFIA¿ PC with V3.0 Software 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· 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