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. 1,867 recalls have been distributed to Kansas in the last 12 months.
Showing 23161–23180 of 28,538 recalls
Recalled Item: Monaco radiation therapy treatment planning system. The Monaco system is...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Electric Pen Drive (EPD) System Recalled by Synthes, Inc. Due to In...
The Issue: In May 2013, the original recall was initiated due to complaints the Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...
The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...
The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...
The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...
The Issue: The devices were not shipped with the Starter Kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...
The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...
The Issue: Transmitter may initiate a software reset resulting in backup operation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...
The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...
The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo (cold) Laser Desktop Control Units Recalled by Pivotal Health...
The Issue: Control units were equipped with an internal mounting kit that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...
The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul Femoral Head - A modular head component is used Recalled by Zimmer...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...
The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.