ClearanceBrief
Recall Z-0397-2014 ยท JXG Shunt, Central Nervous System And Components

Medtronic Neurosurgery

CSF-Unitized Shunt, Contoured Regular, Low Pressure, Catalog No. 46022; CSF-Unitized Shunt, Contoured Regular, Medium Pressure, Catalog No. 46024; CSF-Unitized Shunt, Contoured Regular, High Pressure, Catalog No. 46026. CSF-Unitized Shunt Kits are designed as integrated CSF-Flow Control Shunts for use in shunting cerebrospinal fluid from the lateral ventricle of the brain into the peritoneal cavi

DateNov 26, 2013 (initiated Nov 18, 2013)
StatusTerminated
ReasonMedtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt Assembly Kit, and the Strata II Shunt Assembly Kit because they were found to have label discrepancies.
Root causeOther
ActionMedtronic Neurosurgery sent an Urgent Medical Device Recall letter dated November 18, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were advised to provide a copy of the letter to all those who need to be aware of the matter within their organization or to any organization where the potentially affected product may have been transferred. Customers with questions were instructed to call 805-571-8725.
Quantity288 units total (147 units in US)
DistributionWorldwide Distribution - USA (nationwide) and Internationally to US and worldwide: Austria, Belgium, Bosnia, Herzegovina, Canada, Croatia, Germany, Japan, Poland, Portugal, Taiwan, United Arab Emirates, United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K792005CSF-CARDIAC/PERITONEAL CATHETER
Pudenz-Schulte Medical Research Corp., Jan 16, 1980
K792007CSF-VENTRICULAR CATHETER, STANDARD DES
Pudenz-Schulte Medical Research Corp., Jan 16, 1980
K841442P-S MEDICAL CSF-FLOW CONTROL VALVE-
P-S Medical, Apr 19, 1984