Date Initiated by Firm | February 09, 2004 |
Date Posted | February 18, 2004 |
Recall Status1 |
Terminated 3 on January 04, 2005 |
Recall Number | Z-0539-04 |
Recall Event ID |
28264 |
PMA Number | P990013 |
Product Classification |
Intraocular Lens - Product Code HQL
|
Product | Collamer UV One-Piece IntraOcular Lens.
Models 4205BF and 4204BF |
Code Information |
No codes apply |
Recalling Firm/ Manufacturer |
Staar Surgical Co Inc 1911 Walker Ave Monrovia CA 91016-4846
|
For Additional Information Contact | Janice L. Filippelli 626-303-7902 |
Manufacturer Reason for Recall | Risk of hyperopic refractive changes. |
FDA Determined Cause 2 | Other |
Action | Firm is distributing letters to physicians suggesting ways to mitigate the observed contracture of the eye tissues after implantation. Letters will be sent 2/9/2004. |
Quantity in Commerce | No quantity applies. |
Distribution | Nationwide and to Australia, Canada, Chile, France, Germany, India, Lebanon, South Africa, Switzerland, United Kingdom. |
Total Product Life Cycle | TPLC Device Report |
|
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
|
PMA Database | PMAs with Product Code = HQL
|