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. 1,831 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,831 in last 12 months

Showing 3242132440 of 50,914 recalls

Medical DeviceOctober 14, 2016· Covidien LLC

Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...

The Issue: Sterility of the outer surface of the container compromised due to packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Reshape Medical Inc

Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...

The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
DrugOctober 13, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: due to out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2016· Pharmedium Services, LLC

Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Alere San Diego, Inc.

Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...

The Issue: Encoded with incorrect ranges that are not consistent with the ranges...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Baxter Healthcare Corp.

Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...

The Issue: Potential presence of particulate matter on the blood side of the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

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

Class II — Potential Health HazardOngoing