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Terminated

SurgiFrost Cryosurgical Probes

FDA Recall Z-0728-03 · Posted 2003-04-16

Recalling FirmEndocare Inc
Recall StatusTerminated
Product CodeGEH
Date Initiated2002-10-25
Date Terminated2003-04-15
Product Quantity933

Reason for Recall

Device design failure, connectivity.

Firm Action

This recall has been completed. Recall notice was sent by fax on October 25, 2002.

Root Cause

Other

Distribution Pattern

Product was sent only to one Canadian distribution company whoin turn sold it internationally and back to the USA.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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