| Date Initiated by Firm | December 14, 2006 |
| Date Posted | February 15, 2007 |
| Recall Status1 |
Terminated 3 on April 09, 2008 |
| Recall Number | Z-0429-2007 |
| Recall Event ID |
37009 |
| PMA Number | P040020 |
| Product Classification |
Intraocular Lens - Product Code MFK
|
| Product | AcrySof ReSTOR Intraocular Lens |
| Code Information |
Model SN60D3, Serial numbers: 968290.039; 934317.012; 934317.013; and 948332.080. |
| FEI Number |
1610287
|
Recalling Firm/ Manufacturer |
Alcon Laboratories, Inc
6201 South Fwy
Fort Worth
TX
76134-2001
|
Manufacturer Reason for Recall | Intraocular lenses exposed to extreme temperatures while in storage. |
FDA Determined Cause 2 | Other |
| Action | The recall of the fifteen re-shipped lenses was conducted by telephone calls to the nine customers that had received the lenses. These calls were made on December 14, 2006. |
| Quantity in Commerce | 4 units |
| Distribution | Nationwide. |
| 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 = MFK
|