FDAOctober 27, 2022device

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer

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

The hazard

There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

1080190216290510801902141030108019021595921080190216291210801902159110108019022031581080190214104710801902140675

Recall history

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

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