Medfusion Syringe Pump recall
Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump.
Why was Medfusion Syringe Pump recalled?
Inaccurate delivery can occur following an interrupted Bolus or Loading dose, if a specific sequence of events occurs.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 Numbers: 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82. Software Version V6.0
- Product
- Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump.
- Recalling firm
- Smiths Medical ASD Inc.
- Quantity
- 17019 units
- Distribution
- Worldwide distribution - United Arab Emirates, United States, Afghanistan, Albania, Australia, Belgium, Bermuda, Canada, China, Germany, Denmark, Great Britain, Hong Kong, Indonesia, Ireland, India, Korea, Kuwait, Lebanon, Mexico, Malaysia, New Zealand, Oman, Panama, Philippines, Pakistan, Poland, Saudi Arabia, Trinidad and Tobago
- Recall date
- August 12, 2020
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)