Becton Dickinson Infusion Therapy Systems, Inc.: Device Recall
Recall #Z-1808-2025 · 04/21/2025
Recall Details
- Recall Number
- Z-1808-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Becton Dickinson Infusion Therapy Systems, Inc.
- Status
- Ongoing
- Date Initiated
- 04/21/2025
- Location
- Sandy, UT, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 262,800
Reason for Recall
Due to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV to be placed - which may result in therapy delay.
Product Description
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
Distribution Pattern
Worldwide - US Nationwide distribution in the states of IN, AL, CA, FL, TX, NJ, MO, NC, NY, OH, AZ, MN, MA, WA, OK, KS, MS, LA, MD, GA, TN, NM, PA and the country of CA.
Other Recalls by Becton Dickinson Infusion Therapy Systems, Inc.
- Class II: Risk 05/21/2025
- Class II: Risk 05/21/2025
- Class II: Risk 05/21/2025
- Class II: Risk 05/21/2025
- Class II: Risk 05/21/2025
View all recalls by Becton Dickinson Infusion Therapy Systems, Inc. →