Triton FP Infusion Pump — Class II medical device recall Z-1122-2014
Terminated recall by WalkMed Infusion, LLC, reported 2014-03-12, distributed in IL, KS, MA, NJ. WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part Number 400000 due to the label o
| Recall number | Z-1122-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | WalkMed Infusion, LLC, Englewood, CO, United States |
| Recall initiated | 2014-02-17 |
| Classified | 2014-03-03 |
| Reported by FDA | 2014-03-12 |
| Terminated | 2014-10-06 |
| Distributed | IL, KS, MA, NJ |
| Quantity | 797 |
| Reason classes | labeling |
| Model numbers | 400000 |
Product
Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospitals, ambulatory & nursing home (extended care) settings, and home care environments.
Reason for recall
WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part Number 400000 due to the label on the right side of the pump containing an incorrect instruction.
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-1122-2014. 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.