RecallRadar

FDA Device recall Z-0630-2026

Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pum…

On 2025-12-03 the FDA classified a Class II recall of Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pum… by B Braun Medical, citing potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0630-2026
ClassificationClass II
Statusongoing
Initiated2025-10-29
Published2025-12-03
Last updated2026-09-13 11:57 UTC
CompanyB Braun Medical
Distributionn/a

Product

Extension 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 numbers: 1. EXTENSION SET, 18 IN; Catalog Number: 490448. 2. EXTENSION SET, 52 IN.; Catalog Number: 490465. 3. EXTENSION SET 49 IN.; Catalog Number: 490486. 4. EXTENSION SET, 12 CARESTITE LADS; Catalog Number: 490577.

Reason

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

Identifiers

code_info
1. Catalog Number: 490448; Primary UDI-DI: 04046964848858; Unit of Dose UDI-DI: 04046964848841. Shelf Life: Earliest Ex…1. Catalog Number: 490448; Primary UDI-DI: 04046964848858; Unit of Dose UDI-DI: 04046964848841. Shelf Life: Earliest Exp of Comp or 36mths. 2. Catalog Number: 490465; Primary UDI-DI: 04046964950735; Unit of Dose UDI-DI: 04046964950728. Shelf Life: Earliest Exp of Comp or 36mths. 3. Catalog Number: 490486; Primary UDI-DI: 04046964991257; Unit of Dose UDI-DI: 04046964991240. Shelf Life: Earliest Exp of Comp or 24mths. 4. Catalog Number: 490577; Primary UDI-DI: 04046955287536; Unit of Dose UDI-DI: 04046955287529. Shelf Life: Earliest Exp of Comp or 36mths.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0630-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.