Becton Dickinson Infusion Therapy Systems, Inc.: FDA recalls

FDA enforcement reports name Becton Dickinson Infusion Therapy Systems, Inc. as the recalling firm in 7 events. The events have 15 product records. The recalls started from 2021 to 2025. All the events are device recalls.

See the 7 events

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Enforcement events

7 events, newest first.

FDA enforcement events of Becton Dickinson Infusion Therapy Systems, Inc.
Initiated	Product (first record)	Type	Class	Records	Status
21 May 2025	REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY	Device	Class II	9	Ongoing
21 Apr 2025	BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC, REF: 386803; BD Cathena Safety IV Catheter BD Multiguard Technology 20 GA x 1.00 IN, 386862	Device	Class II	1	Ongoing
26 Jun 2024	BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be inserted into a patient's peripheral vascular system for short term use to sample blood, monitor blood pressure, or…	Device	Class II	1	Ongoing
4 Oct 2023	BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533	Device	Class II	1	Ongoing
29 Aug 2023	REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO	Device	Class II	1	Ongoing
12 Oct 2022	BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)	Device	Class II	1	Ongoing
8 Sep 2021	BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660 mL/hr)-0.5mL, REF 383536; BD Q-Style Luer Access Split Septum BD Vialon Material; BD Instaflash Needle Technology; Rx Only, Sterile EO. BD Nexiva closed IV catheter systems are over-the-needle,…	Device	Class II	1	Ongoing

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

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Type and class

Becton Dickinson Infusion Therapy Systems, Inc.: events for each product type
Type		Events
Device		7

Becton Dickinson Infusion Therapy Systems, Inc.: events in each class
Class		Events
Class II		7

Share of the events of the firm in Class I: 0%
Share of all events on the register in Class I: 18%
Events with the status Ongoing: 7

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Becton Dickinson Infusion Therapy Systems, Inc., by the year that the recall started. The largest year is 2023, with 2 events.

Official channels

FDA enforcement reportsThe FDA search of the weekly enforcement reports.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA: report a problemThe FDA page that shows where a report about a product goes.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Cite this page

Recall Register. Becton Dickinson Infusion Therapy Systems, Inc.: FDA recalls. https://recallregister.com/firm/becton-dickinson-infusion-therapy-systems-inc/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
State of the firm address: UT

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Becton Dickinson Infusion Therapy Systems, Inc. have?: Class II: 7 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Becton Dickinson Infusion Therapy Systems, Inc.?: FDA event 96865, which the firm started on 21 May 2025. The first product in the record is: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
How many FDA recalls of Becton Dickinson Infusion Therapy Systems, Inc. have the status Ongoing?: 7 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.