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Centurion Medical Products Recalls

152 recalls on record · December 18, 2013 to July 15, 2020 · Medical Devices

Recalls by year

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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Neonatal Cap Change Kit DT20315
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Cap Change Kit DT20310
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls PORT AND IO ACCESS DRESSING KIT DT15780A
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls CVC BUNDLE WITHOUT CATH CVI4600
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls NEONATAL PROCEDURE TRAY PICC CATHETERS CVI4535
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls PEDIATRIC PICC INSERTION TRAY CVI4450A
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls PEDIATRIC PICC INSERTION TRAY CVI4450
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls PICC Line Accessory Kit CVI4285
Hazard: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls SNAG FREE SUTURE TRAY Kit Code: SUT14355 - Product Usage: Kit is used for laceration repairs for general population.
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls LACERATION TRAY Kit Code: SUT18370 - Product Usage: Kit is used for laceration repairs for general population.
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls UNIVERSAL BLOCK TRAY Kit Code: MNS6645 - Product Usage: Kit is used for regional anesthesia nerve blocks for general pop
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Usage: Kit is used for Driveline Maintenance and Secure
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls DRIVELINE MANAGEMENT TRAY Kit Code: DT17780B - Product Usage: Kit is used for Driveline Maintenance and Securement of Li
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls HIGH DRAINAGE LVAD TRAY Kit Code: DM950 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line fo
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for ge
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls LVAD DRESSING SYSTEM W/BIOPATCHKit Code: DM700 - Product Usage: Kit is used for Left Ventricular Assist Device Dressing
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - Product Usage: Kit is used for Peripheral Central Line Insertion proced
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls CIRCUMCISION TRAY Kit Code: CIT2650H - Product Usage: Kit is used for performing circumcision procedures on newborns.
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is used for performing circumcision procedures on newborns.
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls STERILE FLUORO SSP TRAY Kit Code: MNS11605 - Product Usage: This kit is used for arthrogram injection and aspiration. Th
Hazard: Potential for sterile packaging to be compromised
August 14, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of t
Hazard: Potential for sterile packaging to be compromised
August 7, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Hazard: Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.
June 12, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Sterile Nail Nipper, Barrel Spring (I68400), Sterile
Hazard: Compromised seal on the sterile barrier pouch.
June 12, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Sterile Nail Clipper Concave Edge (67710)
Hazard: Compromised seal on the sterile barrier pouch.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls WOUND CLOSURE TRAY - FACIAL
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls WOUND CARE KIT
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls EXCISION TRAY
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls NEONATAL IV START KIT
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls INFANT IV SECUREMENT KIT
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls IV START KIT
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.