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. 2,557 recalls have been distributed to Oregon in the last 12 months.
Showing 17381–17400 of 28,488 recalls
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: 88" (224 cm) Y-Type Blood Set w/200 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 159" (404 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 119" Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due to Some...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100" (254 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 120" (305cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 32" (81 cm) Appx 4.4 mL Recalled by ICU Medical, Inc. Due to Some devices...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Y-Type Blood Set with 170 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 84" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 125" (318 cm) Bifuse Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
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: 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: 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: 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: 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.