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. 2,499 recalls have been distributed to Oregon in the last 12 months.
Showing 22781–22800 of 50,914 recalls
Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer Recalled by Inopak Ltd Due to...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Instant Waterless Hand Sanitizer Recalled by Inopak Ltd Due to CGMP...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INODERM Antiseptic Hand Soap (E-2) Recalled by Inopak Ltd Due to CGMP...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX Recalled by Inopak Ltd...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unison Hand Care Products Recalled by Inopak Ltd Due to CGMP Deviations:...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...
The Issue: Images may potentially become corrupt while using the system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...
The Issue: Reports of aspirating biopsy needle breakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.