FDA Recall Terminated

Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.

Recall: Z-0989-2014 · Initiated December 23, 2013

Recall

Recall Number
Z-0989-2014
Event Number
67174
Firm
Aesculap, Inc.
FEI Number
2916714
Product Code
JXG
Status
Terminated
Root Cause
Employee error
Initiated
December 23, 2013
Posted
February 19, 2014
Terminated
October 1, 2014
Address
3773 Corporate Pkwy, Center Valley, PA, 18034-8217

Description

Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.

Reason

The accuracy is out of specification for the Aesculap proSA Adjustment Disc Size L.

Action

Aesculap sent an Important Correction and Removal Notification dated December 23, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customers.. Yom"Aesculap Sales Representative will contact you to schedule a time to remove the FV795T from Set FV792T. Please use FV790T in the absence of the FV795T to ensure the correct adjustment has been made. Please complete the attached Inventory Sheet which is necessary to comply with FDA regulations. When completing the inventory sheet, please fill in the quantity being returned. If you cannot locate the product, please provide an explanation as to why the inventory will not be returned (discarded, etc.). AIC (USA) appreciates your cooperation on this matter and apologizes for the inconvenience this may cause. Thank you for your patience and continued support of this product. Please call (610) 984-9265 or (610) 984-9414 with any questions.

Distribution

Worldwide Distribution - US Distribution including the states of AZ, MD, MA, WI, MI, MN, DE, KS, and FL., and the countries of Australia, Germany, Great Britain, Norway and Japan.

Quantity

79