AcrySof ReSTOR Intraocular Lens
This recall has been terminated (originally issued February 15, 2007).
- Company
- Alcon Laboratories, Inc
- Recall Initiated
- December 14, 2006
- Posted
- February 15, 2007
- Terminated
- April 9, 2008
- Recall Number
- Z-0430-2007
- Quantity
- 10 units
- Firm Location
- Worth, TX
- Official Source
- View on FDA website ↗
Reason for Recall
Intraocular lenses exposed to extreme temperatures while in storage.
Distribution
Nationwide.
Lot / Code Info
Model MN60D3, Serial numbers: 940376.028; 945173.084; 945533.043; 945174.053; 944089.027; 942202.069; 940407.058; 940407.059; 942210.016; and 945537.073
Root Cause
Other
Action Taken
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.
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AcrySof ReSTOR Intraocular Lens
Feb 15, 2007
AcrySof Intraocular Lens
Feb 15, 2007