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. 2,447 recalls have been distributed to Oregon in the last 12 months.
Showing 34161–34180 of 50,914 recalls
Recalled Item: Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz....
The Issue: Product did not meet specifications for Zinc Acetate (OOS).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specification; 9 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical portio adapter (acorn) small & large are used for Recalled by...
The Issue: The distal end of the Conical portio adapter (acorn) is composed of a small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vari-Safe Injection Needle US endoscopy 5976 Heisley Road Mentor Recalled by...
The Issue: US Endoscopy is conducting a voluntary product recall of one lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...
The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.