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. 2,655 recalls have been distributed to Oregon in the last 12 months.
Showing 5841–5860 of 50,914 recalls
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BSM-3000 Series Bedside Monitor The Life Scope BSM-3000 Recalled by Nihon...
The Issue: Due to software issue the device may give false "SpO2 Probe Failure" alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: traMADol Hydrochloride Tablets Recalled by Rubicon Research Private Limited...
The Issue: Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CDC Recalled by Centers For Disease Control and Prevention Due to The H5b...
The Issue: The H5b component may fail to amplify, resulting in an inconclusive result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic...
The Issue: Potential for an electrical component of the O-arm" O2 Imaging System to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresh N Lean brand Crustless Chicken Potato Pot Pie. Packaged in plastic...
The Issue: Possible contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MethylPREDNISolone Acetate Injectable Suspension Recalled by Sagent...
The Issue: Presence of Particulate Matter: Potential for black particulates in the drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valacyclovir Tablets USP Recalled by Viatris Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: There is a potential for the imprint,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EsoFLIP Recalled by Covidien, LLC Due to Due to saline conductivity issues,...
The Issue: Due to saline conductivity issues, their is a potential that dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening...
The Issue: Stardrive Screwdrivers manufactured without a 5-degree relief cut around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progesterone 200 mg Recalled by Coast Quality Pharmacy, LLC dba Anazao...
The Issue: Presence of Foreign Substance; Broken metal piece found embedded in tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol decanoate Injection 50mg/mL Recalled by SOMERSET THERAPEUTICS...
The Issue: Presence of Foreign Substance: This oil based product may contain trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted)...
The Issue: Presence of foreign substance: Product complaint of foreign material in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.