Atlas FDA

Gold Hub Capistrano Cannula, Catalog Nos. HK10C15; HK10C23;HK12C15;HK12C23: HK14C15; HK14C23; HK16C5; HK16C8; HK16C12; H

FDA device recall Z-0898-05 · posted 2005-06-17 · Terminated

Recall details

Recalling firm
HK Surgical Inc
Reason for recall
Risk of hubs becoming disconnected from the cannula.
Action taken
Recall letters were sent 12/3/2004, 04/11-14/2005 letters request return of the cannulas.
Root cause
Other
Status
Terminated
Product code
FIE
Quantity affected
To be determined
Distribution
Nationwide, Saudi Arabia, New Zealand, Phillipines, Switzerland, Canada, Netherlands, Taiwan, Germany, Japan, Malaysia, United Kingdom, Indonesia, Austria, Belgium, Puerto Rico, England.
Date initiated
2004-12-03
Date posted
2005-06-17
Date terminated
2012-04-19
Location
San Juan Capistrano, CA

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