Aesculap Miethke Shunt System recall
Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of…
Why was Aesculap Miethke Shunt System recalled?
Aesculap Inc. (AIC (USA)) initiated a recall of Miethke Shunt System accessories due to missing patients' labels for the miniNAV (FV660T). There are no patient injuries resulting from this issue.
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?
Catalog No: FV660T Lot No: 4506022655
- Product
- Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of…
- Recalling firm
- Aesculap, Inc.
- Quantity
- 4
- Distribution
- Distributed in OK, and WI.
- Recall date
- December 24, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)