Alaris Pump Module model 8100
Reported: July 19, 2017 Initiated: June 12, 2017 #Z-2700-2017
Product Description
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.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 35,940 units
- Distribution
- US and Canada
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
Alaris Pump Module model 8100. Recalled by CareFusion 303, Inc.. Units affected: 35,940 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 19, 2017. Severity: Moderate. Recall number: Z-2700-2017.
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