B Braun Medical Inc: Device Recall
Recall #Z-0660-2026 · 10/29/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0660-2026
- 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
- 1,272 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
IV Administration Set 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 number: 1. IV ADMIN SET,2 CARESITE, TRIP MANIFOLD; Catalog Number: 490343.
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
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.