Bausch & Lomb Inc- Greenville Solutions Plant: Medical Device Recall in 2014 - (Recall #: Z-1554-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 21, 2014

Date Posted: May 14, 2014

Recall Number: Z-1554-2014

Event ID: 68095

Reason for Recall:

Out of specification results for one of the two disinfectants.

Status: Terminated

Product Quantity: 256,440 bottles

Code Information:

Lot GK2127 (twin packs), SKU: 623588, GK2131 (twin packs), SKU: 623500, STL2019, (6 pk shelf display containing GK2131, SKU: 629743 and STL2025 (6 pk shelf display containing GK2127), SKU: 629743.

Distribution Pattern:

US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated