Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0713-2026 — SAFELINE 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. UNIVERSAL IV ADMIN SET; Catalog Number: 352604. 2. S

U.S. FDA — Device Enforcement · United States · 2025-10-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0713-2026
Date of alert
2025-10-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
B Braun Medical Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04046964181870
Reported risk: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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