Alaris Pump Module model 8100 — Class II medical device recall Z-2700-2017
Terminated recall by CareFusion 303, Inc., reported 2017-07-19. There is a potential risk that could cause unintended flow in the older, centered sear door latch design in th
| Recall number | Z-2700-2017 |
|---|---|
| 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 | 2017-07-07 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2019-01-28 |
| Countries outside the US | CA |
| Quantity | 35,940 units |
| Model numbers | 8100 |
Product
Alaris Pump Module model 8100
Reason for recall
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
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-2700-2017. 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.