Symbiq One Channel Infuser recall
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa…
Why was Symbiq One Channel Infuser recalled?
The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response, or may register a different value from the value selected by the user. Failure of the touchscreen to respond to user input could result in a delay in therapy or result in over delivery or under delivery of medication if the user does not confirm the programmed values on the pump's confirmation screen prior to starting the infusion.
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?
List Number 16026-01, all serial numbers
- Product
- Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa…
- Recalling firm
- Hospira Inc.
- Quantity
- 19,614 units
- Distribution
- Worldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Canada
- Recall date
- October 31, 2012
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)