Integra PAC1 Mod 2 Cables used with the Integra MPM, CAM01 Monitors
FDA device recall Z-0944-2012 · posted 2012-02-03 · Terminated
Recall details
- Recalling firm
- Integra LifeSciences Corp
- 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.
- Action taken
- 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
- Status
- Terminated
- Product code
- GWM
- Quantity affected
- 221 Units
- Distribution
- Worldwide Distribution-- USA (nationwide ) .
- Date initiated
- 2011-10-20
- Date posted
- 2012-02-03
- Date terminated
- 2013-06-18
- Location
- Plainsboro, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) (K962928) | Camino Neurocare, Inc. | 1996-12-20 |