FDA Recall Terminated

Ventricular Bolt Monitoring Kit W/Cranial Access, Drain, 1104HMC, Integra LifeSciences, 3498 West 2400 South, West Valley City, Utah 84119. Kit contains components which are used to monitor Intra Cranial Pressure and provide access to the cerebral ventricles for Cerebro-spinal fluid sampling, drainage and fluid injection.

Recall: Z-2171-2011 · Initiated February 22, 2011

Recall

Recall Number
Z-2171-2011
Event Number
58216
Firm
Integra LifeSciences Corp.
FEI Number
3003418325
Product Code
HBG
Status
Terminated
Root Cause
Error in labeling
Initiated
February 22, 2011
Posted
May 10, 2011
Terminated
May 10, 2011
Address
311 Enterprise Dr, Plainsboro, NJ, 08536-3344

Description

Ventricular Bolt Monitoring Kit W/Cranial Access, Drain, 1104HMC, Integra LifeSciences, 3498 West 2400 South, West Valley City, Utah 84119. Kit contains components which are used to monitor Intra Cranial Pressure and provide access to the cerebral ventricles for Cerebro-spinal fluid sampling, drainage and fluid injection.

Reason

Outer box of Monitoring Kit was mislabeled with the incorrect part number.

Action

Integra LifeSciences Corp. sent an Urgent Product Recall Notification letter dated February 22, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were asked to quarantine any affected product and arrange for return to Integra by contacting Integra Customer Service Returns at 1-800-654-2873 (choose option 2) to obtain a Return Merchandise Authorization number and place an order for replacement product. Customers were asked to complete the attached "Recall Acknowledgement and Return Form" indicating whether or not they possess any of the product identified. For any questions regarding this recall call 609-936-2485.

Distribution

Nationwide Distribution including CA, CT, GA, HI, IL, KY, MA, NC, NJ, NM. NV, OH, TX, WA, and WI.

Quantity

45 kits