Cardica, Inc. Recalls

Overview of recall records associated with Cardica, Inc., including dates, categories and classifications where available.

2recall records

Dec 30, 2015latest record date

Dec 30, 2015earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceDec 30, 2015

Cardica MicroCutter Xchange 30 Blue Cartridge, FG-025320 recall — FDA Z-0482-2016

Cardica, Inc. has received reports that use of the Blue Cartridges with the MicroCutter XCHANGE 30 Stapler was associated with incomplete firing of staples, potentially resulting in an…

Class IIFDA: TerminatedCardica, Inc.

Medical DeviceDec 30, 2015

Cardica MicroCutter Xchange 30 Blue Curved Tip Cartridge recall — FDA Z-0483-2016

Cardica, Inc. has received reports that use of the Blue Cartridges with the MicroCutter XCHANGE 30 Stapler was associated with incomplete firing of staples, potentially resulting in an…

Class IIFDA: TerminatedCardica, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Cardica, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.