Becton Dickinson Infusion Therapy Systems, Inc. recalls
Every recall we track for Becton Dickinson Infusion Therapy Systems, Inc. — 15 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Becton Dickinson Infusion Therapy Systems, Inc. more than tripled in 2025 (10, up from 1 in 2024). 7% rated “stop using now”.
All FDA recall records for Becton Dickinson Infusion Therapy Systems, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 0 | 0 | 1 |
| 2023 | 0 | 2 | 0 | 0 | 2 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 9 | 1 | 0 | 10 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Becton Dickinson Infusion Therapy Systems, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Becton Dickinson Infusion Therapy Systems, Inc. recalls
7 shown- Lower riskMedical device
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly
Becton Dickinson recalls BD Insyte Autoguard shielded IV catheters due to possible needle failure to retract, which could cause slow or incomplete needle retraction during use.
Becton DickinsonMay 21, 2025 - Use cautionMedical device
Becton Dickinson Infusion Therapy Systems, Inc. recalls BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter
Becton Dickinson recalls BD Cathena Safety IV Catheters with a potential septum hole causing blood leakage during insertion, risking exposure or needing a second IV. Affected models include 18GA x 1.25IN and 20GA x 1.00IN with specific lot numbers.
Becton DickinsonApr 21, 2025 - Lower riskMedical device
Becton Dickinson Infusion Therapy Systems, Inc. recalls BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63
Becton Dickinson recalls BD Insyte Autoguard BC shielded IV catheters with potential leakage during insertion due to tubing holes. Affected units have specific model and lot numbers. Consumers should contact for details.
Becton DickinsonJun 26, 2024 - Use cautionMedical device
Becton Dickinson Infusion Therapy Systems Inc. recalls BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533
Becton Dickinson recalls BD Insyte Autoguard BC Shielded IV Catheters with blood control technology due to potential needlestick injuries from improper needle retraction. Affected units have specific model and lot numbers.
Becton DickinsonOct 4, 2023 - Use cautionMedical device
Becton Dickinson Infusion Therapy Systems Inc. recalls 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
Becton Dickinson recalls BD Cathena Safety IV catheters with potential safety shield failure, risking needle exposure during use. Affected units include specific model and lot numbers.
Becton DickinsonAug 29, 2023 - Stop using nowMedical device
Becton Dickinson Infusion Therapy Systems Inc. recalls 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)
Becton Dickinson recalls specific BD Nexiva IV catheter systems due to risk of needle tip exposure during use. Affected units have catalog number 383516 and were sold in 2023. Consumers should stop using immediately.
Becton DickinsonOct 12, 2022 - Lower riskMedical device
Becton Dickinson Infusion Therapy Systems Inc. recalls 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
Becton Dickinson recalls BD Nexiva IV catheter systems due to non-sterile packaging. This could lead to infections if used without proper sterility. Affected units have specific batch numbers and model numbers.
Becton DickinsonSep 8, 2021
Becton Dickinson Infusion Therapy Systems, Inc. recall questions
How many recalls has Becton Dickinson Infusion Therapy Systems, Inc. had?
15 recalls from Becton Dickinson Infusion Therapy Systems, Inc. are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Becton Dickinson Infusion Therapy Systems, Inc. recall?
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly, dated May 21, 2025. Every Becton Dickinson Infusion Therapy Systems, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Becton Dickinson Infusion Therapy Systems, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Becton Dickinson Infusion Therapy Systems, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.