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Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOn
Recalled July 2, 2025 · FDA recall Z-2006-2025 · 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: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 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 →