Alaris PC Unit — Class II medical device recall Z-2671-2017
Terminated recall by CareFusion 303, Inc., reported 2017-07-12, distributed nationwide. BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result
| Recall number | Z-2671-2017 |
|---|---|
| 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 | 2017-06-12 |
| Classified | 2017-07-03 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2018-10-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, NZ, ZA |
| Quantity | 568,283 units |
| Model numbers | 8015 |
Product
Alaris PC Unit, Model 8015
Reason for recall
BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potentially result in interrupted infusions.
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-2671-2017. 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.