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. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 19781–19800 of 50,914 recalls
Recalled Item: Garlic Parmesan Sauce Recalled by Golden State Foods Due to Notification by...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Bell Creamy Jalapeno Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Hut Garlic Dipping Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colonel's Coleslaw Dressing Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...
The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...
The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...
The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity core Recalled by Roche Diagnostics Operations, Inc. Due to...
The Issue: Alarm flags that have a "<" symbol in front of them are not displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Garbanzo Beans are sold under different brands and described Recalled by...
The Issue: 11.8 ppm of glyphosate was detected in dry garbanzo beans.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The 13 Bean Soup Mix product is distributed in 2000 Recalled by Columbia...
The Issue: Product was recalled due to a potential for contamination with glyphosate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.