Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,886 recalls have been distributed to Kansas in the last 12 months.
Showing 20621–20640 of 28,538 recalls
Recalled Item: Vaxcel PICC with PASV IR-145 Kit under the following labels: 1) 4F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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 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: 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: 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: 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: Drew Scientific Inc. Drew3-PAC. This D3 Reagent Pack includes: diluent...
The Issue: The reagent pack may result in elevated platelet background during Drew3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCareCoordinator allows the customer to schedule patient tasks (i.e....
The Issue: The adherence check generates a software error. Two issues occur as a result...
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: All instrumentation associated with the Prelude PF Resurfacing Knee System....
The Issue: Inadequate design control.
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: 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: 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: 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.
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.