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Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381433, BD Insyte Autoguard Shielded IV Catheter, 20GA x 1.00 in (1.1x25 mm) 65 mL/min, STERILEEO, RxOnly
Recalled July 2, 2025 · FDA recall Z-2002-2025 · Becton Dickinson Infusion Therapy Systems
Hazard
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. · FDA Class II
Units
50 units
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, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Belgium, Canada, Chile, Colombia, Guatemala, Japan, New Zealand, Panama, Philippines, Singapore, Vietnam.
Description
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Product
REF: 381433, BD Insyte Autoguard Shielded IV Catheter, 20GA x 1.00 in (1.1x25 mm) 65 mL/min, STERILEEO, RxOnly
Manufacturer(s)
Becton Dickinson Infusion Therapy Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →