Atlas FDA

Staarvisc II Sodium Hyaluronate 0.8 mL 12mg/mL Syringe. Sterile. Rx. For intraocular use. P/N490-001 Distributed by: STA

FDA device recall Z-0109-04 · posted 2003-11-13 · Terminated

Recall details

Recalling firm
Anika Therapeutics
Reason for recall
Stability failure at the 20 month for viscosity specification
Action taken
Anika Therapeutics issued notification on 10/8/2003 by fax and FedEx to three Distributors. Distributors were requested to subrecall to their customers.
Root cause
Other
Status
Terminated
Product code
LZP
Quantity affected
1526 units
Distribution
CA, MO, NC,VA
Date initiated
2003-10-08
Date posted
2003-11-13
Date terminated
2004-08-09
Location
Woburn, MA

Monitor recalls programmatically

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