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. 2,511 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,511 in last 12 months

Showing 2088120900 of 50,914 recalls

Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Tablets USP Recalled by AuroMedics Pharma LLC Due to CGMP...

The Issue: CGMP DEVIATIONS: One lot of Ranitidine Tablets USP, 150 mg is being recalled...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Himasal Natural Nasal Saline Solution Recalled by Unipharma, Llc. Due...

The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Morton Grove...

The Issue: Failed Impurities/Degradation Specifications - failed specs for Prednisolone...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Children's Natural Cough Syrup English Ivy Leaf Recalled by...

The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Potential for calibration error resulting in QC failures after the...

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

Class II — Potential Health HazardOngoing