RecallWatchUSA

Home / Brands / Centurion Medical Products

Centurion Medical Products Recalls

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

Recalls by year

13
14
15
16
17
18
19
20

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

November 6, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Kit, Port Access Product Code: DYNDC1582A
Hazard: Supplier initiated recall of the GRIPPER Needles
November 6, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Maintenance Flush Kit/Blood Draw Product Code: DT19335
Hazard: Supplier initiated recall of the GRIPPER Needles
November 6, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Port full Access Tray Product Code: DT19330
Hazard: Supplier initiated recall of the GRIPPER Needles
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Centurion CIRCLAMP W/1.3 CM BELL-single-use, disposable instrument used to compress the foreskin of the penis during ci
Hazard: A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls Centurion CIRCLAMP W/1.1CM BELL - single-use, disposable instrument used to compress the foreskin of the penis during c
Hazard: A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
October 16, 2019Medical DevicesFDA
Centurion Medical Products Corporation recalls UVC TRAY UVT875
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 TRIPLE LUMEN CVC 20CM BUNDLE STCVC2040
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 INVASIVE PROCEDURE TRAY MNS9510
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 IV KIT - SORBAVIEW IVS3475
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 IV SECUREMENT KIT IVS3405
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 IV START KIT IV8440
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 VANTEX 7FR, 16CM, 3L CVC BUNDLE ECVC6670
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 OR VANTEX 7FR 3L 16CM CVC ECVC6665
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 CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A
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 CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545
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 CENTRAL LINE BUNDLE ECVC6375
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 INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355
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 TRIPLE LUMEN SAFETY BUNDLE ECVC6070
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 VANTEX 7F, 3L, 20CM ECVC6065
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 MULTIMED, 3L, 20CM ECVC6060
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, 20CM, 3L, PI ECVC5120A
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, 20CM, 3L, PI ECVC5120
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, 20CM, 4L, PI ECVC5095
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 CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
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 TRIPLE LUMEN BUNDLE KIT ECVC1540
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 BUNDLE KIT DYNDC2137
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 STERILE CAP CHANGE KIT DYNDC1946B
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 INFUSA PORT KIT DYNDC1840F
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 INFUSA PORT KIT DYNDC1840E
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 DYNDC1496B
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.