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. 2,454 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,454 in last 12 months

Showing 3362133640 of 50,914 recalls

Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to The product contained a...

The Issue: The product contained a latex catheter instead of a silicone catheter.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: Option-vm Urinary Catheter. Male use only. Latex Free. Sterile Recalled by...

The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: Option-vf Urinary Catheter. Female use only. Latex Free. Sterile Recalled by...

The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Operating Table TruSystem 7000 U Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Mobile Column TruSystem 7500 Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Floor Mounting Column TS 7500 U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Stationary Column TruSystem 7599 Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
FoodJuly 8, 2016· Montana Flour & Grains, Inc

Recalled Item: 100% Organic Spelt Grain Recalled by Montana Flour & Grains, Inc Due to...

The Issue: Organic Spelt Grain is recalled because label does not declare wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 8, 2016· Montana Flour & Grains, Inc

Recalled Item: 100% Organic Unbleached White Flour Recalled by Montana Flour & Grains, Inc...

The Issue: Organic Unbleached White Flour is recalled because label does not declare wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 8, 2016· Montana Flour & Grains, Inc

Recalled Item: 100% Organic Spelt Flour Recalled by Montana Flour & Grains, Inc Due to...

The Issue: Organic Spelt Flour is recalled because label does not declare wheat.

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

Class II — Potential Health HazardOngoing
Refund