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Terminated

Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.

FDA Recall Z-1554-2014 · Posted 2014-05-06

Recalling FirmBausch & Lomb Inc- Greenville Solutions Plant
Recall StatusTerminated
Product CodeLYL
Date Initiated2014-04-21
Date Terminated2015-01-09
Product Quantity256,440 bottles

Reason for Recall

Out of specification results for one of the two disinfectants.

Firm Action

Consignees were notified via registered mail starting 04/21/2014.

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K083757BPZ02 MULTIPURPOSE SOLUTIONBausch & Lomb, Inc. · 2009-11-18

Official Source

View FDA Recall →

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

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