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. 2,565 recalls have been distributed to Kansas in the last 12 months.
Showing 13081–13100 of 28,538 recalls
Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...
The Issue: Problem with packaging sealing process which affects sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...
The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...
The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...
The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...
The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...
The Issue: Reports have been received of the CentriMag Systems experiencing motor and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.