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. 2,637 recalls have been distributed to Oregon in the last 12 months.
Showing 10001–10020 of 28,488 recalls
Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 1.0 ml Recalled by ICU Medical, Inc. Due to Due to molding defect,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 4.1 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer - Product Usage: Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Admin Set w/ClaveTM Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Abre Venous Self-expanding Sent System Recalled by Medtronic Inc....
The Issue: Incorrect size printed on the device; packaging is labeled correctly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...
The Issue: May have been programmed with a less than optimal brightness setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...
The Issue: bioMerieux received complaints about calibration issue observed on several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...
The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...
The Issue: Stryker identified non-conforming instruments that are components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.