Alaris PC units — Class II medical device recall Z-1311-2015
Terminated recall by CareFusion 303, Inc., reported 2015-04-01, distributed nationwide. CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on du
| Recall number | Z-1311-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2015-03-12 |
| Classified | 2015-03-23 |
| Reported by FDA | 2015-04-01 |
| Terminated | 2017-09-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, SG |
| Quantity | 56,015 units |
| Serial numbers | 13728944, 13728945, 13729599, 13729644, 13729773, 13729802, 13729812, 13729853, 13729867, 13729931, 13729967, 13730147, 13730159, 13730194, 13730239, 13730304, 13730314, 13730374, 13730396, 13730402, 13730407, 13730477, 13730509, 13730560, 13730600 and 475 more |
| Model numbers | 8015 |
Product
Alaris PC units, Model No. 8015. Infusion pump.
Reason for recall
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
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-1311-2015. 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.