Acuvue Advance for Astigmatism Diagnostic Product. Expected Primary Package Label: Lot B0077KM 3.75D 1.7cyl. 180 Axis Ex
FDA device recall Z-2012-2009 · posted 2009-09-18 · Terminated
Recall details
- Recalling firm
- Vistakon
- Reason for recall
- Vistakon is recalling Acuvue Advance for Astigmatism Diagnostic product for mislabeling.
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- LPL
- Quantity affected
- 73
- Distribution
- Nationwide.
- Date initiated
- 2009-04-20
- Date posted
- 2009-09-18
- Date terminated
- 2009-10-01
- Location
- Jacksonville, FL
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