Recall Z-0071-2008
Neomedix Corp · initiated May 28, 2007
Product
NeoMedix Trabectome I/A Console, Model Number 550014, surgical aspirator
Codes / lots: Model Number 550014; Lot Number 061205-1; Serial Numbers: 10117, 10119, 10120, 10122, 10124, 100129, and 10133.
Reason for recall
Failure of irrigation flow: The pinch valve in a few pumps may not consistently open to allow irrigation flow. In over 450 surgeries, the firm confirmed one instance of a valve that did not open. The electrically activated pinch valve in the NeoMedix Trabectome I/A pump activates irrigation flow to the eye during Trabectome surgery.
FDA-determined cause: Nonconforming Material/Component
Action taken
On May 31, 2007 NeoMedix mailed a Customer letter to all consignees informing them of the hazard. The letter also indicated to the customers they NeoMedix has developed a minor modification/upgrade that is designed to assure that the pinch valve opens at the appropriate time. The customers were instructed this modification requires return of their existing pump for modification and testing at the firm's facility before its return. In the event that surgeries have already been scheduled, NeoMedix will provide a loaner unit until the suspect unit can be modified and returned to you. The letter also indicated the cost of the modification and/or use of a loaner unit will be entirely at NeoMedix expense. You will be contacted to establish the details of implementing this modification.
Details
- Recall number
- Z-0071-2008
- Initiated
- May 28, 2007
- Posted by FDA
- September 29, 2008
- Terminated
- September 29, 2008
- Product code
- BTA – Pump, Portable, Aspiration (Manual Or Powered)
- Quantity
- 7
- Distribution
- Nationwide to: CA, HI, IA, NY & PA
- Recalling firm
- Neomedix Corp, Tustin, CA