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. 2,681 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,681 in last 12 months

Showing 32213240 of 50,914 recalls

DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2025· Stryker Corporation

Recalled Item: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture Recalled by...

The Issue: Increase in complaints concerning "pullwire" breakage that may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: Pentax Medical Video Processor- Intended to be used with PENTAX Recalled by...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: PENTAX Medical Video Upper GI Scope-Intended to provide optical...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: PENTAX Medical Video Colonoscope- Intended to provide optical visualization...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate Recalled...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Optima XR646 HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Definium 656HD & Discovery XR656HD (GTINs: 00840682138598 Recalled by GE...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656 HD. X-Ray imaging system. Recalled by GE Medical Systems,...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing