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. 1,087 recalls have been distributed to Oregon in the last 12 months.
Showing 15641–15660 of 50,914 recalls
Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...
The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles...
The Issue: Presence of Foreign Substance: Potential for broken glass within the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems Recalled...
The Issue: The high and low level "Quality Controls" demonstrate a positive bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...
The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.