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. 2,470 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,470 in last 12 months

Showing 2608126100 of 50,914 recalls

Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D V Recalled by Siemens Medical Solutions USA, Inc Due to In rare cases of...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...

The Issue: QFix has advised Mevion Medical Systems that they are identifying...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: If the beam model has a highly asymmetric primary source, it is not...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2018· PFIZER

Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...

The Issue: Microbial Contamination of Sterile Products: Product associated with reports...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2018· LUPIN SOMERSET

Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...

The Issue: Subpotent Drug and Failed Content Uniformity.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2018· Pinnacle Food Group, Llc

Recalled Item: Wish Bone House Italian Salad Dressing 15 oz. Recalled by Pinnacle Food...

The Issue: The recall was initiated after learning from a retail customer that a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 28, 2018· Datex-Ohmeda, Inc.

Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...

The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2018· Envoy Medical Corporation

Recalled Item: Final Pack Recalled by Envoy Medical Corporation Due to Sterile Wipes packed...

The Issue: Sterile Wipes packed in these four Esteem II Sound Processors had an earlier...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2018· Genicon, Inc.

Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...

The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Elekta Instrument AB

Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...

The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing