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. 2,432 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,432 in last 12 months

Showing 3746137480 of 50,914 recalls

Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Beckman Coulter Inc.

Recalled Item: Access Free T3 Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...

The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2015· VRVK Nutraceuticals, LLC

Recalled Item: DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT...

The Issue: The dietary supplement contains undeclared milk and crustacean shellfish...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 27, 2015· The One Minute Miracle Inc

Recalled Item: MIRACLE DIET 30 capsules Recalled by The One Minute Miracle Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 27, 2015· The One Minute Miracle Inc

Recalled Item: MIRACLE ROCK 48 capsules Recalled by The One Minute Miracle Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 27, 2015· Nutraceutical International Corporation

Recalled Item: KAL Brand Amino Acid Complex Recalled by Nutraceutical International...

The Issue: Undeclared allergen, casein is a disclosed ingredient, but the word milk not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 27, 2015· Becton Dickinson & Co.

Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of tests associated with the affected lots(...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....

The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2015· Zimmer, Inc.

Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...

The Issue: Product labeling of these sterile guide wires (external carton label and...

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

Class II — Potential Health HazardOngoing