CareFusion Recalls Alaris Pump Module 8100 Due to Latch Design Risk
CareFusion 303, Inc. is recalling 35,940 Alaris Pump Module model 8100 units in the US and Canada due to a potential risk of unintended flow caused by the sear door latch design.
- Product
- Alaris Pump Module model 8100
- Category
- Medical Device
- Distribution
- 0 states