Hydroline Trumpet Valve — Class II medical device recall Z-2495-2018
Terminated recall by Cardinal Health 200, LLC, reported 2018-07-25, distributed in AL, AR, AZ, CA, CO, DC, DE, FL…. The suction valve may not close properly which could cause continuous suction.
| Recall number | Z-2495-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health 200, LLC, Waukegan, IL, United States |
| Recall initiated | 2018-06-11 |
| Classified | 2018-07-18 |
| Reported by FDA | 2018-07-25 |
| Terminated | 2020-08-17 |
| Distributed | 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 |
| Countries outside the US | BE, DE, FR, GB, IL, IT, NL, SG |
| Quantity | 63,020 valves |
| Lot numbers | 21719, 41738 |
| Model numbers | ASU1221 |
Product
Hydroline Trumpet Valve, Trumpet Valve, No Probe, Double Spike, Ref ASU1221, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
Reason for recall
The suction valve may not close properly which could cause continuous suction.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2495-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.