FDA Device recall Z-1554-2014
Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile
- FDA Device
- Class II
- terminated
- Published 2014-05-14
On 2014-05-14 the FDA classified a Class II recall of Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile by Bausch And Lomb Greenville Solutions Plant, citing out of specification results for one of the two disinfectants.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1554-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-21 |
| Published | 2014-05-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Bausch And Lomb Greenville Solutions Plant |
| Distribution | US |
Product
Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.
Reason
Out of specification results for one of the two disinfectants.
Identifiers
| code_info | Lot GK2127 (twin packs), SKU: 623588, GK2131 (twin packs), SKU: 623500, STL2019, (6 pk shelf display containing GK2131,…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. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2014%22
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