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.
Showing 16621–16640 of 50,914 recalls
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Injection Recalled by Accord Healthcare, Inc. Due to...
The Issue: Labeling; Label Mix-up; correctly labeled 2 mL vials were packaged into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evolve Cell Culture Bags Recalled by OriGen Biomedical, Inc. Due to It was...
The Issue: It was identified that tissue culture bags were incorrectly labeled as free...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope and accessories Recalled by Olympus Corporation of the Americas...
The Issue: Olympus Medical Systems Corporation (OMSC) has received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: think! Protein + Fiber Oatmeal Recalled by Glanbia Performance Nutrition...
The Issue: Undeclared ingredients including but not limited to pecans and almonds
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole Endless Summer Salad Kit Recalled by Dole Fresh Vegetables Inc Due to...
The Issue: Two consumer complaints received for incorrect Master pack in Endless Summer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sensis / Sensis Vibe systems with software version VD12 and Recalled by...
The Issue: System may sporadically freeze (lock-up) during operation or while being in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc...
The Issue: Due to the release of nonconforming Intraocular Lenses (IOLs).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cisatracurium Besylate Injection Recalled by Meitheal Pharmaceuticals Inc...
The Issue: Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to The firm has...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gram-Negative Bacteria And Associated Resistance Markers Recalled by BioFire...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...
The Issue: Product was compromised during shipment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.