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FlowArt®

ASSET MEDIKAL TASARIM SANAYI VE TICARET ANONIM SIRKETI · Model AVV4020 · UDI-DI 08699443585308

LHI Prescription
1
510(k) clearances
14,331
Adverse events (20 deaths)
61
Recalls
173
Facilities

Description

Vial Access Device Vented, 20 mm

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.