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. 2,594 recalls have been distributed to Kansas in the last 12 months.
Showing 9561–9580 of 28,538 recalls
Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...
The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G...
The Issue: Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...
The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...
The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.