FDA Recall Terminated

FS-OMNI, Fusion Omni-Tome, Sterile, Rx only, Wilson Cook Medical, GI Endoscopy, 4900 Bethania Station Road, Winston-Salem, NC 27105, EC Representative: Cook Ireland Ltd, O'Haioran Road, National Technology Park, Limerick, Ireland. The Fusion Omni-Tome is supplied sterile and is a single use device. This device is used in cannulation of the ductal system and for sphincterotomy.

Recall: Z-0325-2009 · Initiated October 30, 2008

Recall

Recall Number
Z-0325-2009
Event Number
50118
Firm
Cook Endoscopy
FEI Number
1037905
Product Code
KNS
Status
Terminated
Root Cause
Process control
Initiated
October 30, 2008
Posted
January 5, 2009
Terminated
April 7, 2009
Address
5951 Grassy Creek Blvd, Winston Salem, NC, 27105-1206

Description

FS-OMNI, Fusion Omni-Tome, Sterile, Rx only, Wilson Cook Medical, GI Endoscopy, 4900 Bethania Station Road, Winston-Salem, NC 27105, EC Representative: Cook Ireland Ltd, O'Haioran Road, National Technology Park, Limerick, Ireland. The Fusion Omni-Tome is supplied sterile and is a single use device. This device is used in cannulation of the ductal system and for sphincterotomy.

Reason

The wire control port may have been omitted during manufacture.

Action

Cook Ireland (distributor) was contacted via email on 10/30/08 and was instructed to contact their customers and coordinate the return of all recall product to Cook Endoscopy. A response sheet was attached. Recall status reports will be issued monthly. All devices returned as part of this recall initiative will be dispositioned to scrap and destroyed. Should you have any questions, please contact Cook Endoscopy Customer Quality Assurance Department at 1-336-744-0157.

Distribution

Ireland

Quantity

11