Quickcable Autoclaveable Cable Electrode Cable
FDA Recall Z-1006-04 · Posted 2004-07-20
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Recalling FirmBiosense Webster, Inc.
Recall StatusTerminated
Product CodeDRF
Date Initiated2004-05-21
Date Terminated2005-03-31
Product Quantity212
Reason for Recall
Mislabeling.
Firm Action
Recall was by letter on May 21, 2004 requesting return of affected lot.
Root Cause
Other
Distribution Pattern
Nationwide, Australia, Korea, Chile, Brazil.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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