PeroxiClear Peroxide Solution — Class II medical device recall Z-0651-2017
Terminated recall by Bausch & Lomb Inc Irb, reported 2016-11-30, distributed nationwide. Product was found to contain excess residual levels of hydrogen peroxide.
| Recall number | Z-0651-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bausch & Lomb Inc Irb, Rochester, NY, United States |
| Recall initiated | 2016-09-19 |
| Classified | 2016-11-21 |
| Reported by FDA | 2016-11-30 |
| Terminated | 2018-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 4,652,822 units |
| UPC / GTIN / UDI-DI | 00310119038154, 00310119038161, 00310119038178, 00310119039083, 00310119039106, 00310119097120 |
| Lot numbers | 2016/09/30, 2016/10/31, 2016/11/30, 2016/12/31, 2017/01/31, 2017/02/28, 2017/03/31, 2017/04/30, 2017/05/31, 2017/06/30, 2017/07/31, 2017/09/30, 2017/10/31, 2017/11/30, 2017/12/31, 2018/01/31, 623815C, 623816B, GA16023ST1, GA16027ST, GA16032ST, GA16036ST, GA16043ST, GA16046ST, GA16052ST, GA16056ST, GA16060ST, GA16072-1, GA16076-1, GC15002ST, GC15008ST, GC15008ST1, GC15012AST, GC15026ST, GC15037ST, GC15044ST, GC15044ST1, GC15049ST, GC15052ST, GC16035ST and 120 more |
| Model numbers | 623815, 623816, 623817, 623908, 623910, 629712 |
Product
PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin Pack for Target stores, 12 oz. for Walmart Vision Center and 3 oz. Starter Kit US), Manufactured by Bausch + Lomb, Rochester, NY 14609. PeroxiClear 3% Hydrogen Peroxide Cleaning & Disinfecting Solution is indicated for the daily cleaning, removal of protein deposits, disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel) and rigid gas permeable contact lenses.
Reason for recall
Product was found to contain excess residual levels of hydrogen peroxide.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0651-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.