Atlas FDA

STAAR Phaco Tubing Kit

FDA device recall Z-0775-05 · posted 2005-04-27 · Terminated

Recall details

Recalling firm
Staar Surgical Co Inc
Reason for recall
Complaints of leaking with question of sterility and risk of infection in eye.
Action taken
Recall was conducted by telephone and letter delivered by FEDEX on April 7, 2004. All consignees have been contacted.
Root cause
Other
Status
Terminated
Product code
GDY
Quantity affected
114
Distribution
CA, NV, UT, FL, OR.
Date initiated
2005-03-28
Date posted
2005-04-27
Date terminated
2005-07-11
Location
Monrovia, CA

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