Recall Z-1725-2011

Millar Instruments, Inc · initiated March 8, 2011

Terminated

Product

Millar Instruments, Inc. Millar Sensors Systems Solutions Mikro-Tip Angiographic Catheters Sterile and Nonpyrogenic Model SPC-454D and SPC454F. Provide intravascular pressure readings and capability for the deliverance of high-speed injection of radiopaque contrast media used in vascular imaging to selected sites in the vascular system.

Codes / lots: 800-4219-1 and 800-4219-3 Listing #: D055900 and D055901

Reason for recall

Possibility of epoxy debris particles inside the catheter lumen.

FDA-determined cause: Process design

Action taken

The firm, Millar, notified their consignees/customers by email and sent hardcopy of email on March 8, 2011. The notification described the product, problem and actions to be taken. The customers were instructed to return the catheter(s) to Millar or report back to Millar if the catheter(s) has been consumed. If you have any questions, please do not hesitate to contact Director, RA/QA at 832-667-7000.

Details

Recall number
Z-1725-2011
Initiated
March 8, 2011
Posted by FDA
March 24, 2011
Terminated
June 27, 2011
Product code
DQO – Catheter, Intravascular, Diagnostic
Quantity
1080 units
Distribution
MN, NY, Washington DC, NC, MA, MN, PA, CA, MI, Australia, Germany, Canada, Japan, United Kingdom, and Norway.
Recalling firm
Millar Instruments, Inc, Houston, TX

Official FDA recall record