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. 2,681 recalls have been distributed to Oregon in the last 12 months.
Showing 1601–1620 of 28,488 recalls
Recalled Item: Product Name: MR 7700 Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Ambition X Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Elition S Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 1.5T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for XR and 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for 1.5T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: MR 5300 Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Upgrade to MR 7700 Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The HemoCue Glucose 201 Microcuvettes are designed for use with Recalled by...
The Issue: Glucose microcuvettes experienced transit time outside of limits, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One+ Continuous Glucose Monitoring System Recalled by Dexcom, Inc....
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One Continuous Glucose Monitoring System Recalled by Dexcom, Inc. Due...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.