Class II — CareFusion 303, Inc.
| Recalling firm | CareFusion 303, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | Alaris Pump Module model 8100 |
| Quantity | 35,940 units |
| Distribution | US and Canada |
| Initiated | 2017-06-12 |
| Classified | 2017-07-07 |
| Terminated | 2019-01-28 |
| Recall number | Z-2700-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — CareFusion 303, Inc. (Z-2700-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77279/
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