B Braun Medical Inc: Device Recall
Recall #Z-0603-2026 · 10/29/2025
Recall Details
- Recall Number
- Z-0603-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- B Braun Medical Inc
- Status
- Ongoing
- Date Initiated
- 10/29/2025
- Location
- Bethlehem, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 43,900 units
Reason for Recall
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Product Description
ADDitIV utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog numbers: 1. Primary Gravity IV Set, 2 Non-Needle-Free Injection Sites; Catalog Number: V1443. 2. ADDITIVE SET W/ 3 INJ SITES -DR*; Catalog Number: V1447. 3. ADD PEDIATRIC 3 INJ LUER LOCK; Catalog Number: V1448. 4. ADULT ADD 2 INJ CKV LUER LOCK; Catalog Number: V1484.
Distribution Pattern
Worldwide distribution - US distribution and international distribution to Canada, Germany, Guatemala, and Singapore.
Other Recalls by B Braun Medical Inc
- Class II: Risk 10/29/2025
- Class II: Risk 10/29/2025
- Class II: Risk 10/29/2025
- Class II: Risk 10/29/2025
- Class II: Risk 10/29/2025