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Terminated

MicroSTAAR Injector Cartridges Models: SFC-25 (utilized with plate haptic Collamer lens) MTC-60 (utilized with plate haptic Silicone lens)

FDA Recall Z-0378-04 · Posted 2004-01-29

Recalling FirmStaar Surgical Co Inc
Recall StatusTerminated
Product CodeKYB
Date Initiated2004-01-06
Date Terminated2005-01-04

Reason for Recall

Increased numbers of lens tears during placement of lens into eye.

Firm Action

Customers will recieve recall notice, Customer Bulletin and MicroStaar Injector Cartridge Guide by Federal Espress (sent 1/6/04).

Root Cause

Other

Distribution Pattern

Nationwide, Canada and Australia

Official Source

View FDA Recall →

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

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