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. 1,090 recalls have been distributed to Kansas in the last 12 months.
Showing 9101–9120 of 28,538 recalls
Recalled Item: BF-1T60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-P180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...
The Issue: There is a potential for distal end of catheters to fracture and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...
The Issue: Revised Instructions for Use: Potential for specimens from patients with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoGel 100 - RED Medical Supplies Green Ultrasound Gel Recalled by Red...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Recalled...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LikoStretch 1900 Model Number: 3156051 - The combination of this Recalled by...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch Leveller Model Number: 3156200 - The combination of this Recalled by...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.