FDA recall Z-2700-2017
CareFusion 303, Inc. · Class II · device
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.
Distribution
US and Canada
Key facts
- Status
- Terminated
- Initiation date
- 2017-06-12
- Report date
- 2017-07-19
- Termination date
- 2019-01-28
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- San Diego, CA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2700-2017