RecallRadar

FDA Device recall Z-2337-2017

ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation

On 2017-06-21 the FDA classified a Class II recall of ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation by Arrow International, citing the Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limite….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2337-2017
ClassificationClass II
Statusterminated
Initiated2017-05-09
Published2017-06-21
Last updated2026-09-13 11:54 UTC
CompanyArrow International
DistributionUS

Product

ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation

Reason

The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to: -multiple infusions of fluids, medications, or chemotherapy -infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values -frequent blood sampling or blood/blood components infusions -infusion of incompatible medications -central venous pressure monitoring lack of usable peripheral IV sites -replacement of multiple peripheral sites for IV access

Identifiers

code_infoMaterial number: CDC-24301-1A, CDC-24306-1A Device Listing D025398

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2337-2017%22

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