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. 1,103 recalls have been distributed to Kansas in the last 12 months.
Showing 3141–3160 of 28,538 recalls
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to Recalled by B Braun...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TxHA PEEK IBF/TxTiHA IBF System i. TxHA The Recalled by Innovasis, Inc Due...
The Issue: Due to interfacing issues between the implant trial and inserter of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser Systems-Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser - Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Sheath Introducer 7.5F Recalled by Merit Medical Systems, Inc. Due...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seer Home System is an ambulatory electroencephalograph (EEG) system...
The Issue: During CAPA investigations of sight production inconsistencies, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vios Monitoring System Bedside Monitor Model BSM2050 Recalled by Murata...
The Issue: Batteries may deplete over time while not in use if devices are stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILIZABLE INTERNAL DEFIBRILLATION PADDLES STERILIZABLE INTERNAL...
The Issue: Due to customer complaints and out of box failures, the firm is conducting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or Recalled...
The Issue: Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewPoint 6 Recalled by GE Healthcare GmbH Due to The National Institute of...
The Issue: The National Institute of Standards and Technology (NIST) has identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.