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. 2,475 recalls have been distributed to Oregon in the last 12 months.
Showing 23481–23500 of 28,488 recalls
Recalled Item: Additional devices identified in new FSN MA-FCO 83000190: QLAB versions...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile drape Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...
The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items...
The Issue: The blade retaining clip may be difficult to engage and thereby increase the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM PERMANENT CAUTERY HOOK Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM RESANO FORCEPS Recalled by Intuitive Surgical, Inc. Due to Deviations in...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.