Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear — Class II medical device recall Z-2916-2018
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2018-08-29, distributed nationwide. Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears
| Recall number | Z-2916-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Johnson & Johnson Vision Care, Inc., Jacksonville, FL, United States |
| Recall initiated | 2018-07-23 |
| Classified | 2018-08-23 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2021-12-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | BB, CA, JP, KR |
| UPC / GTIN / UDI-DI | 00733905577215, 00733905615078, 00733905888472 |
| Lot numbers | 516191, 5165910101, 5165910102, 5165910103, 5165910104, 5165910105, 5165910106, 5165910107, 5165910108, 5165910109, 5165910110, 5165910111, 5165910112, 5165915101, 5165915110 |
Product
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes who may have 1.00D or less of astigmatism.
Reason for recall
Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears to the customer or consumer as visibly smaller in diameter, thicker/stiffer to the touch and more darkly tinted blue than the normal contact lens.
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-2916-2018. 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.