MedStream Programmable Infusion Pump- Implantable for recall
MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200.…
Why was MedStream Programmable Infusion Pump- Implantable for recalled?
Miscalibrated Fill Level Sensor may affect dosing level
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?
All serial numbers
- Product
- MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200.…
- Recalling firm
- Codman & Shurtleff, Inc.
- Quantity
- 2 units US and 735 OUS
- Distribution
- Worldwide Distribution-USA (nationwide) including the states of FL, NC, NJ, and TX, and the countries of Austria, Belgium, Spain, Great Britain, Germany, Italy, Ireland, Luxemburg, Russia, Saudi Arabia, Portugal, Greece, Egypt, Switzerland, and Turkey.
- Recall date
- July 24, 2013
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)