Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

STAAR Phaco Tubing Kit

FDA Recall Z-0775-05 · Posted 2005-04-27

Recalling FirmStaar Surgical Co Inc
Recall StatusTerminated
Product CodeGDY
Date Initiated2005-03-28
Date Terminated2005-07-11
Product Quantity114

Reason for Recall

Complaints of leaking with question of sterility and risk of infection in eye.

Firm Action

Recall was conducted by telephone and letter delivered by FEDEX on April 7, 2004. All consignees have been contacted.

Root Cause

Other

Distribution Pattern

CA, NV, UT, FL, OR.

Official Source

View FDA Recall →

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

↑