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 24001–24020 of 28,538 recalls
Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...
The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Aria Implant Inserter Recalled by Stryker Spine Due to Stryker has...
The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty Aria Inserter Recalled by Stryker Spine Due to Stryker has...
The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...
The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling
The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.