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FLEBOSET

LABORATORIOS GRIFOLS SA · Model DOUBLE · UDI-DI 08426314792578

LHI Prescription
10
510(k) clearances
14,331
Adverse events (20 deaths)
61
Recalls
173
Facilities

Description

FLEBOSET DOUBLE is a disposable transfer set through which substances form 2 different vials containing the same solution may be continuously delivered for: a) IV administration when used in conjunction with a gravity or pump infusion set, with luer-lock connection to the drip chamber, to cannel the solution from the source vials to the infusion set, and b) Pharmacy compounding when used in conjuntion with the Grifill pharmacy compounding device and associated transfers sets. Equipped with a spike on each line and a 0.2um hydrophobic air-filter, it minimizes teh formation of aerosols when preparing/dispensing the source substances.

Recalls

DateFirmReason
2025-02-20Omnicell, Inc.IVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during se
2024-09-24West Pharmaceutical Services AZ, Inc.Due to packaging damage from heat exposure during shipping/transportation that may result in a breach in the sterile barrier.
2024-08-20Baxter Healthcare CorporationBaxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H9
2024-08-20Baxter Healthcare CorporationBaxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H9
2024-08-20Baxter Healthcare CorporationBaxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H9
2024-08-20Baxter Healthcare CorporationBaxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H9
2023-12-22Baxter Healthcare CorporationAn error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in
2023-12-22Baxter Healthcare CorporationAn error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in
2022-09-16International Medical Industries, Inc.Blister package had an unsealed edge compromising sterility.
2022-07-14Baxter Healthcare CorporationThere is a potential for leaking valves on ports 1 to 4 in certain lots of valve sets.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.