Recall
FDAHealthOctober 29, 2025

B Braun Medical Inc — 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.

⚠️ Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
October 29, 2025

Worldwide distribution - US distribution and international distribution to Canada, Germany, Guatemala, and Singapore.

What's affected?

Product
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. SAFELINE ADDITIV ALTVTD 3 INJ S; Primary Gravity IV Set with 3 SafeLine Injection Sites; Catalog Number: NF1251. 3. SAFELINE PED. ADDITIVE; Primary Gravity IV Set with 3 SafeLine Injection Sites; Catalog Number: NF1290.
Lot code
1. Catalog Number: 352604; Primary UDI-DI: 04046964181870; Unit of Dose UDI-DI: 04046964181863; Expiration Date: Earliest Exp of Comp or 60mths. 2. Catalog Number: NF1251; Primary UDI-DI: 04046964187100; Unit of Dose UDI-DI: 04046964187094; Expiration Date: Earliest Exp of Comp or 60mths. 3. Catalog Number: NF1290; Primary UDI-DI: 04046964187148; Unit of Dose UDI-DI: 04046964187131; Expiration Date: Earliest Exp of Comp or 60mths.

Additional details

1. Catalog Number: 352604; Primary UDI-DI: 04046964181870; Unit of Dose UDI-DI: 04046964181863; Expiration Date: Earliest Exp of Comp or 60mths. 2. Catalog Number: NF1251; Primary UDI-DI: 04046964187100; Unit of Dose UDI-DI: 04046964187094; Expiration Date: Earliest Exp of Comp or 60mths. 3. Catalog Number: NF1290; Primary UDI-DI: 04046964187148; Unit of Dose UDI-DI: 04046964187131; Expiration Date: Earliest Exp of Comp or 60mths.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 46,250 units.

View original FDA notice →

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