Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl. oz. (30 ml), Bausch & Lomb Incorporated, Rochester, NY 14609.
FDA Recall Z-1735-2009 · Posted 2009-08-13
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Recalling FirmBausch & Lomb Inc
Recall StatusTerminated
Product CodeLPN
Date Initiated2009-06-30
Date Terminated2012-05-10
Product Quantity56,000 bottles
Reason for Recall
The product failed to meet one of the shelf life specifications at the end of the expiry period.
Firm Action
Bausch & Lomb issued an "Urgent Voluntary Medical Device Recall" notice dated June 26, 2009. All consignees were requested to review their inventory, and return any of the affected product to Stericycle Pharmaceutical Services, Indianapolis, IN. A Business Reply Card was included to be returned to Bausch & Lomb via US mail. A prepaid UPS Packing Slip was also provided to return the affected product.
For further questions, contact Bausch & Lomb Customer Resource Center at 1-800-828-9030.
Root Cause
Other
Distribution Pattern
Nationwide Distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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