FDA Device recall Z-2491-2018
Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile
- FDA Device
- Class II
- terminated
- Published 2018-07-25
On 2018-07-25 the FDA classified a Class II recall of Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, 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
| Agency | FDA Device |
|---|---|
| Recall number | Z-2491-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-11 |
| Published | 2018-07-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cardinal Health 200 |
| Distribution | AL, 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 33cm Probe, Double Spike, Ref ASU1201, 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_info | Lot numbers 31712, 31711, 31713, 31714, 31764, 31765, 41711, 41713, 41715, 41724, 41737, 41714, 41721, 41722, 41723, 41…Lot numbers 31712, 31711, 31713, 31714, 31764, 31765, 41711, 41713, 41715, 41724, 41737, 41714, 41721, 41722, 41723, 41727, 41726, 41725, 41719, 41731, 41732, 41730, 41728, 41733, 41734, 41735, 71738, 71739, 71740, 71748, 71741, 71742, 81745, and 71743. |
|---|
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-2491-2018%22
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