FDA Recall
Terminated
Gold Hub Finesse Cannula, Catalog Nos. HK10F23; HK12F10; HK12F15; HK12F23; HK14F10; HK14F15; HK14F23; HK16F5; HK16F8
Recall: Z-0899-05
·
Initiated December 3, 2004
Recall
- Recall Number
- Z-0899-05
- Event Number
- 31878
- Firm
- HK Surgical Inc
- FEI Number
- 1000125732
- Product Code
- FIE
- Status
- Terminated
- Root Cause
- Other
- Initiated
- December 3, 2004
- Posted
- June 17, 2005
- Terminated
- April 19, 2012
- Address
- 30280 Rancho Viejo Rd, San Juan Capistrano, CA, 92675-1561
Description
Gold Hub Finesse Cannula, Catalog Nos. HK10F23; HK12F10; HK12F15; HK12F23; HK14F10; HK14F15; HK14F23; HK16F5; HK16F8
Reason
Risk of hubs becoming disconnected from the cannula.
Action
Recall letters were sent 12/3/2004, 04/11-14/2005 letters request return of the cannulas.
Distribution
Nationwide, Saudi Arabia, New Zealand, Phillipines, Switzerland, Canada, Netherlands, Taiwan, Germany, Japan, Malaysia, United Kingdom, Indonesia, Austria, Belgium, Puerto Rico, England.
Quantity
To be determined