Atlas FDA

Quickcable Autoclaveable Cable Electrode Cable

FDA device recall Z-1006-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Biosense Webster, Inc.
Reason for recall
Mislabeling.
Action taken
Recall was by letter on May 21, 2004 requesting return of affected lot.
Root cause
Other
Status
Terminated
Product code
DRF
Quantity affected
212
Distribution
Nationwide, Australia, Korea, Chile, Brazil.
Date initiated
2004-05-21
Date posted
2004-07-20
Date terminated
2005-03-31
Location
Irwindale, CA

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