Johnson & Johnson Vision Care, Inc. recalls
Every recall we track for Johnson & Johnson Vision Care, Inc. — 8 in all, from 2017–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Johnson & Johnson Vision Care, Inc. peaked in 2017 (4); 8 since 2017.
All FDA recall records for Johnson & Johnson Vision Care, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 4 | 0 | 4 |
| 2018 | 0 | 1 | 0 | 0 | 1 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Johnson & Johnson Vision Care, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Johnson & Johnson Vision Care, Inc. recalls
6 shown- Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Johnson & Johnson Vision Care recalls ACUVUE OASYS MAX 1-Day Multifocal contact lenses with bubbles/voids found during testing. Consumers should check product details to determine if affected.
Johnson & Johnson Vision CareJun 12, 2025 - Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
Johnson & Johnson Vision Care recalls ACUVUE VITA daily contact lenses with Base Curve 8.8 and Refractive Power -1.50 due to potential incomplete packaging seals. Consumers should check UPC 733905989612 and lot number BOOWWWL.
Johnson & Johnson Vision CareMay 6, 2021 - Use cautionMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.
Johnson & Johnson recalls specific ACUVUE OASYS for Astigmatism lenses due to incomplete packaging seals. Check lot B00RWF0 and UPC 733905669460.
ACUVUEMar 11, 2019 - Use cautionMedical device
Johnson & Johnson Vision Care, Inc. recalls Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12
Johnson & Johnson Vision Care recalls 1-Day ACUVUE MOIST Daily Wear contact lenses with a partially formed lens that may appear smaller, thicker, and darker blue. Consumers should check lot numbers and contact the company for remedy.
Johnson & Johnson Vision CareJul 23, 2018 - Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
Johnson & Johnson Vision Care recalls ACUVUE OASYS contact lenses with lot number B00NKM0G due to potential package integrity failure observed during testing. Consumers should check their lenses for the specific lot number and model details.
Johnson & Johnson Vision CareDec 18, 2017 - Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
Johnson & Johnson Vision Care recalls ACUVUE ADVANCE contact lenses with HYDRACLEAR due to foreign matter complaints between blister and foil. Affected lots include B00DHLP (exp 08/2018) and L002FNL (exp 07/2020).
Johnson & Johnson Vision CareOct 19, 2017
Johnson & Johnson Vision Care, Inc. recall questions
How many recalls has Johnson & Johnson Vision Care, Inc. had?
8 recalls from Johnson & Johnson Vision Care, Inc. are on record with U.S. safety agencies, from 2017–2025.
What is the most recent Johnson & Johnson Vision Care, Inc. recall?
Johnson & Johnson Vision Care, Inc. recalls ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL, dated Jun 12, 2025. Every Johnson & Johnson Vision Care, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Johnson & Johnson Vision Care, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Johnson & Johnson Vision Care, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.