FDAClass IIMay 14, 2014

Bausch & Lomb recall

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

Why was Bausch & Lomb recalled?

Out of specification results for one of the two disinfectants.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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.

Product
Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.
Recalling firm
Bausch & Lomb Inc- Greenville Solutions Plant
Quantity
256,440 bottles
Distribution
US Nationwide.
Recall date
May 14, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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