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 2644126460 of 28,488 recalls

Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Fresenius Medical Care Holdings, Inc. dba Renal Solutions

Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...

The Issue: Product is being recalled because the combination of the current 50 mg vial,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2013· Sysmex America, Inc.

Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...

The Issue: The current Century Break patch did not contain the same setting for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...

The Issue: Correction to provide clarification and additional labeling to minimize...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Transonic Systems Inc

Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...

The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Custom Spine, Inc.

Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...

The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Abbott Molecular

Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...

The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: NeuraWrap Nerve Protector NeuraWrap Nerve Protector is indicated for the...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Ora Plug Absorbable Collagen Wound Dressing for Dental Surgery The Recalled...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: HeliTape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: OraMem Absorbable Collagen Membrane OraMem¿ Absorbable Collagen Membrane is...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: DuraGen XS Dural Regeneration Matrix DuraGen XS Dural Regenerative Matrix...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: BioMend Absorbable Collagen Membrane BioMend¿ Absorbable Collagen Membrane...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Layershield Adhesion Barrier Matrix Layershield Adhesion Barrier Matrix is...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: NeuraGen Nerve Guide NeuraGen Nerve Guide is indicated for repair Recalled...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Absorbable Collagen Sponge Provided As Intermediate to Another Company...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing