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. 1,854 recalls have been distributed to Kansas in the last 12 months.
Showing 24621–24640 of 28,538 recalls
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) Recalled...
The Issue: Software issues with ACUSON SC2000 ultrasound with software version 3/5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...
The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...
The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...
The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....
The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt...
The Issue: AIC (USA) received information regarding 3 complaints in which the deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...
The Issue: Out of specification results for one of the two disinfectants.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...
The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...
The Issue: High priority alert icon was not displayed in the Study List when there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...
The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDFILL Syringe Strip Recalled by Baxter Corporation Englewood Due to...
The Issue: Possible breach in sterile barrier for inner and outer bags of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...
The Issue: This Lot has variations in melting temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...
The Issue: DePuy Synthes is initiating a recall of certain lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.