Atlas FDA

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

FDA device recall Z-0378-04 · posted 2004-01-29 · Terminated

Recall details

Recalling firm
Staar Surgical Co Inc
Reason for recall
Increased numbers of lens tears during placement of lens into eye.
Action taken
Customers will recieve recall notice, Customer Bulletin and MicroStaar Injector Cartridge Guide by Federal Espress (sent 1/6/04).
Root cause
Other
Status
Terminated
Product code
KYB
Distribution
Nationwide, Canada and Australia
Date initiated
2004-01-06
Date posted
2004-01-29
Date terminated
2005-01-04
Location
Monrovia, CA

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.