Alaris PC units, Model No. 8015. Infusion pump.
Reported: April 1, 2015 Initiated: March 12, 2015 #Z-1311-2015
Product Description
Alaris PC units, Model No. 8015. Infusion pump.
Reason for Recall
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 56,015 units
- Distribution
- Worldwide Distribution - USA (nationwide), Canada, European Union, Singapore and Australia.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
Alaris PC units, Model No. 8015. Infusion pump.. Recalled by CareFusion 303, Inc.. Units affected: 56,015 units.
Why was this product recalled? ▼
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 1, 2015. Severity: Moderate. Recall number: Z-1311-2015.
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