FDAOctober 4, 2019device

REF: Z3239, 126" 10 Drop Primary Set w/3 MicroClave, 2 Gang 4-Way Stopcocks, Rotating Luer, 1 Ext, Sterile R, UDI: (01)00887709030473

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential that IV administration sets contain a 15 drops/mL drop cannula instead of a 10 drops/mL drop cannula within the drip chamber. An infusion set with an incorrect drop cannula could result in inaccurate delivery of the intended infusion volume (under-delivery). This could result in under-delivery of critical medication which may lead to serious adverse health consequences.

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

UPCs

00887709030473

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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