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FDA (Device enforcement)Recalled 2024-01-30class ii

Angiodynamics, Inc.: MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750

Hazard

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Details from the source

Reason for recall: Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case Distribution: Worldwide distribution - US Nationwide and the countries of AT, CA, CH, CZ, ES, HK, KW, NL, NO, NZ, ZA. Quantity: 4366 units Lot/code info: UDI: 15051684022934 UPN: H965457501 Lot Number: 5784035 5784036 5784136 5787837 5788554 5788555 5789978 5790448 5790449 5791589 5791590 5791591 5797460 5797461 5798838 5799613 5799623 5800399 5804390 5806116

UPC codes

15051684022934

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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