Integra PAC1 Mod 2 Cables used with the Integra MPM, CAM01 Monitors
FDA Recall Z-0944-2012 · Posted 2012-02-03
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Recalling FirmIntegra LifeSciences Corp
Recall StatusTerminated
Product CodeGWM
Date Initiated2011-10-20
Date Terminated2013-06-18
Product Quantity221 Units
Reason for Recall
Some of the connector cables associated with Integra's intracerebral pressure (ICP) monitors may cause temporary interference with the ICP waveform on the monitor display.
Firm Action
Integra sent a Urgent Product Recall Notification letter dated October 20, 2011, via FedEx, email, and fax to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
The customer was instructed to examine their inventory at your earliest convenience. If you have an effected PAC1 cable, please complete the attached Recall Acknowledgement Form and return it to Integra Customer Service per the instructions on the form. An Integra Sales Representative will contact you to assist in the return and replacement of new cables at no cost.
In the meanwhile, you may continue to use the cables until you have been contacted and replacement product has been provided. Distortion of the ICP wave form can be stopped or prevented by keeping the PACI catheter receptacle out of human contact.
Please contact Integra Customer Service at 1-800-654-2873.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide Distribution-- USA (nationwide ) .
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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