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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 27621–27640 of 50,914 recalls
Recalled Item: Clopidogrel Tablets Recalled by International Laboratories, LLC Due to...
The Issue: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...
The Issue: The power supply unit may be damaged and may fail to start up when the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...
The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Covered Vanilla Ice Cream Bars packaged under the following...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ice Cream Variety Packs containing Sandwiches Recalled by Fieldbrook Foods...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE Recalled by Fieldbrook Foods...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orange Cream Ice Cream Bars sold under the following labels: Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lovastatin Tablets USP Recalled by AVKARE Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin and Sulbactam for Injection 1.5 g vial Recalled by Aurobindo...
The Issue: Presence of Particulate Matter: A confirmed customer report was received for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas...
The Issue: The previous version of method sheets for the Acetaminophen assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Anti HBc Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Gastrin Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge Recalled by Siemens...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Mass Creatine Kinase (MMB) Flex¿ reagent cartridge Recalled...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.