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. 1,019 recalls have been distributed to Kansas in the last 12 months.
Showing 18581–18600 of 50,117 recalls
Recalled Item: Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ Recalled...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vein Irrigation Cannula with blunt tip. ASY BIC Recalled by LivaNova USA...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed Release Capsules USP Recalled by Dr. Reddy's...
The Issue: Discoloration: product contains brown pellets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: R.E.C.K. (Ropivacaine Recalled by QuVa Pharma, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...
The Issue: The thermo switches in the three-phase transformer, which normally aid in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...
The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.