Alcon Laboratories, Inc AcrySof ReSTOR Intraocular Lens Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AcrySof ReSTOR Intraocular Lens
Brand
Alcon Laboratories, Inc
Lot Codes / Batch Numbers
Model SN60D3, Serial numbers: 968290.039, 934317.012, 934317.013, and 948332.080.
Products Sold
Model SN60D3, Serial numbers: 968290.039; 934317.012; 934317.013; and 948332.080.
Alcon Laboratories, Inc is recalling AcrySof ReSTOR Intraocular Lens due to Intraocular lenses exposed to extreme temperatures while in storage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Intraocular lenses exposed to extreme temperatures while in storage.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026