FDAFDA · Food and drugs·Recall number Z-1554-2014
Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.
Published May 14, 2014 · Recall initiated: April 21, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Out of specification results for one of the two disinfectants.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Bausch & Lomb Inc- Greenville Solutions Plant
- Distributor
- US Nationwide.
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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