Staarvisic II Sodium Hyaluronate, 0.8 mL
FDA Recall Z-1106-05 · Posted 2005-08-06
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Recalling FirmStaar Surgical Co Inc
Recall StatusTerminated
Product CodeLZP
Date Initiated2005-07-18
Date Terminated2012-07-25
Product Quantity16,464
Reason for Recall
Sterility may be compromised.
Firm Action
Recall will be communicated by telephone, email and letter. A fax back form will be used to track response and to identify ammount on hand.
Root Cause
Other
Distribution Pattern
Nationwide, Canada and Puerto Rico
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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