Becton Dickinson Infusion Therapy Systems, Inc.

11 FDA enforcement actions

11 Total Recalls

0 Class I

11 Class II

0 Class III

Firm Details

Product Types: device
States: UT

All Recalls

Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 05/21/2025 device

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class II: Risk 04/21/2025 device

Due to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV to be placed - which may result in therapy delay.
Class II: Risk 06/26/2024 device

Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.