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. 1,067 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,067 in last 12 months

Showing 17381–17400 of 50,914 recalls

Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number:...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Recalled...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) Model Number:...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
DrugOctober 30, 2020· AVKARE Inc.

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2020· Prytime Medical Devices, Inc.

Recalled Item: PryTime Medical - ER-Reboa Plus Catheter Recalled by Prytime Medical...

The Issue: There is a potential that catheters may have incorrectly marked balloon and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...

The Issue: Control lots may not meet stability criteria and could result in increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...

The Issue: Control lots may not meet stability criteria and could result in increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva...

The Issue: Calibrator lots may not meet stability criteria and could result in...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2020· Teva Pharmaceuticals USA

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Dissolution Specifications: Out-of-specification dissolution results...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2020· Sunstar Americas, Inc.

Recalled Item: Paroex (chlorhexidine gluconate) Oral Rinse Recalled by Sunstar Americas,...

The Issue: Microbial Contamination of Non-sterile Products: contamination with...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg Recalled by...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2020· Mani, Inc. - Kiyohara Facility

Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...

The Issue: Dimensions of the Luer connector parts out of specification, may cause...

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

Class II — Potential Health HazardOngoing