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 28881–28900 of 50,914 recalls
Recalled Item: Central Venous Tray Triple Lumen Polyurethane Catheter Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns Recalled by...
The Issue: Undeclared eggs
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cobas 8000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A software failure may incorrectly set the system settings to "default"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Brainlab AG Due to Risk of unintended...
The Issue: Risk of unintended motion while the AIRO system is in transport mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female Recalled...
The Issue: Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convertors Robotic Drape with Attached Leggings Recalled by Cardinal Health...
The Issue: Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter; stainless steel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.