Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Reported: March 23, 2016 Initiated: February 15, 2016 #Z-1179-2016
Product Description
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Reason for Recall
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 5,760 units
- Distribution
- Michigan
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007. Recalled by CareFusion 303, Inc.. Units affected: 5,760 units.
Why was this product recalled? ▼
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 23, 2016. Severity: Moderate. Recall number: Z-1179-2016.
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