Acuvue Advance for Astigmatism Diagnostic Product. Expected Primary Package Label: Lot B0077KM 3.75D 1.7cyl. 180 Axis Exp. 2014/07. Actual Primary Package Label: Lot B007NV5 7.50D 1.75cyl. 20 Axis Exp. 2014/12. Product was provided to Eye Care professionals to use as diagnostic replenishment. Product used by Eye Care professionals in the fitting process.
This recall has been terminated (originally issued September 18, 2009).
- Company
- Vistakon
- Recall Initiated
- April 20, 2009
- Posted
- September 18, 2009
- Terminated
- October 1, 2009
- Recall Number
- Z-2012-2009
- Quantity
- 73
- Firm Location
- Jacksonville, FL
- Official Source
- View on FDA website ↗
Reason for Recall
Vistakon is recalling Acuvue Advance for Astigmatism Diagnostic product for mislabeling.
Distribution
Nationwide.
Lot / Code Info
B007NV51 and B0077KM1.
Root Cause
Other
Action Taken
Firm notified consignees by phone from April 7, 2009 to April 27, 2009. Firm requested product disposition. Direct questions about the recall to Vistakon by calling 1-904-443-1763.