Alaris Extension Sets with microbore tubing recall
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…
Why was Alaris Extension Sets with microbore tubing recalled?
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model 20022 Lot Numbers 16087775, Model 20022 Lot Numbers 16127995 and Model 30914 Lot Numbers 16127518 and 17097167
- Product
- 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…
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 25,400 units
- Distribution
- US Distribution to states of: CA, IL, IN, KS, NE, NJ, TX, UT, VA and WA
- Recall date
- June 13, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)