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Terminated

AcrySof Intraocular Lens

FDA Recall Z-0431-2007 · Posted 2007-02-15

Recalling FirmAlcon Laboratories, Inc
Recall StatusTerminated
Product CodeMFK
Date Initiated2006-12-14
Date Terminated2008-04-09
Product Quantityone unit

Reason for Recall

Intraocular lenses exposed to extreme temperatures while in storage.

Firm 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.

Root Cause

Other

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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