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. 2,567 recalls have been distributed to Oregon in the last 12 months.
Showing 16481–16500 of 50,914 recalls
Recalled Item: ExacTrac Dynamic (Medical Charged-Particle Radiation Therapy System)....
The Issue: In case of a failed automatic marker detection, a software error causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...
The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Item #140804 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #140952 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #140946 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...
The Issue: Siemens has become aware of a potential issue in which the imaging system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...
The Issue: Erroneously high FeNO levels which may contribute to premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...
The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOCARE Medical Recalled by Biocare Medical, LLC Due to Their is a potential...
The Issue: Their is a potential that the automated staining instrument with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.