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 20541–20560 of 28,488 recalls
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After importing segmentation results of the left atrium created on the Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...
The Issue: Integra's post QA release review of historical product release test results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...
The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...
The Issue: The units have been fitted with a potentially faulty power supply cable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID...
The Issue: There is a potential problem with the cuvette where failure of the cuvette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 15801 Neonatal...
The Issue: There is a potential problem with the cuvette where failure of the cuvette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET Recalled...
The Issue: There is a potential problem with the cuvette where failure of the cuvette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIgH-Flo Subcutaneous Safety Needle Sets Recalled by Repro-Med Systems, Inc....
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to If the PDM is...
The Issue: If the PDM is utilized to output a pressure for computing fractional flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...
The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...
The Issue: Panorama Central Station including the work station View Station, View...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...
The Issue: The firm received two customer complaints local Pelton & Crane distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.