Becton Dickinson Infusion Therapy Systems, Inc. 2025-07-02 Health serious FDA
Health · FDA · Recall #FDA-Z-2007-2025
REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60… Recall
Issued July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc.
In July 2025, Becton Dickinson Infusion Therapy Systems, Inc. recalled the REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
What you should do
- 1 Stop using REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Becton Dickinson Infusion Therapy Systems, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Becton Dickinson Infusion Therapy Systems, Inc.
- Category
- Health
- Recall date
- July 2, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI
- Recall number
- FDA-Z-2007-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Becton Dickinson Infusion Therapy Systems, Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.