# FDA recall Z-2489-2018

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2018-06-11.

## Product

Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Double Spike and no Probe, Ref ASC1221, 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.

## Distribution

Distribution was made to 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, and WY.  Government and military distribution was also made.  Foreign distribution was made to Belgium, France, Germany, Israel, Italy, Netherlands, Singapore, and United Kingdom.

## Key facts

- **Recall number:** Z-2489-2018
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-11
- **Report date:** 2018-07-25
- **Termination date:** 2020-08-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukegan, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2489-2018

## Citation

> AI Analytics. FDA recall Z-2489-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2489-2018. Source: US FDA. Licensed CC0.

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