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. 2,511 recalls have been distributed to Oregon in the last 12 months.
Showing 19321–19340 of 28,488 recalls
Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...
The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm w/straight Ball Tip Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Guide Rod/950 mm with Smooth Tip Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Guide Rod w/Smooth Tip 950 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...
The Issue: Medtronic has identified an increased number of complaints from customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm Recalled by Synthes (USA) Products LLC Due to The...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod with Ball Tip & Extension/950 mm Recalled by Synthes...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Drug Infusion System. This system...
The Issue: Medtronic is following up to a May 2013 communication regarding the Priming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...
The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4205 Journey Rolling Walker Product Usage: used to assist people in walking...
The Issue: Nova Medical is recalling the Journey Rolling Walker because the screws used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Infusion Pump Recalled by Bayer Healthcare Due to The Source...
The Issue: The Source Administration Sets (SAS) used with the Medrad Intego PET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumex Recalled by GF Health Products, Inc Due to GF Health Products, Inc.,...
The Issue: GF Health Products, Inc., in conjunction with OKIN America, has initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...
The Issue: The insert and case label description of the device incorrectly reads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.