Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.
Reported: June 13, 2018 Initiated: November 6, 2017 #Z-2111-2018
Product Description
Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.
Reason for Recall
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 25,400 units
- Distribution
- US Distribution to states of: CA, IL, IN, KS, NE, NJ, TX, UT, VA and WA
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.. Recalled by CareFusion 303, Inc.. Units affected: 25,400 units.
Why was this product recalled? ▼
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 13, 2018. Severity: Moderate. Recall number: Z-2111-2018.
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