RecallRadar

FDA Device recall Z-2492-2018

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile…

On 2018-07-25 the FDA classified a Class II recall of Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile… by Cardinal Health 200, citing the suction valve may not close properly which could cause continuous suction.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2492-2018
ClassificationClass II
Statusterminated
Initiated2018-06-11
Published2018-07-25
Last updated2026-09-13 11:54 UTC
CompanyCardinal Health 200
DistributionAL, AR, AZ, CA, CO, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MI, MN, MO, MT, NC, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WY

Product

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile. .

Reason

The suction valve may not close properly which could cause continuous suction.

Identifiers

code_infoLot numbers 41774 and 71724.

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-2492-2018%22

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