Johnson & Johnson Vision Care, Inc.
Johnson & Johnson Vision Care, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2021, with 10 FDA device recalls on record.
Top product codes for Johnson & Johnson Vision Care, Inc.
FDA recalls by Johnson & Johnson Vision Care, Inc.
- Z-2163-2025 — ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
- Z-1865-2021 — ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
- Z-1131-2019 — ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.
- Z-2916-2018 — 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.
- Z-1744-2020 — ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
- Z-1211-2018 — 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
- Z-1209-2018 — ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
- Z-1210-2018 — ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
- Z-1335-2013 — 1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. The Vistakon (etafilcon A) Soft (hydrophilic) Contact Lens, Clear and Tinted (Visibility and/or Cosmetically), with UV Blocker for Daily Disposable Wear (spherical) is indicated for daily wear to enhance or alter the apparent color of the eye and/or for the correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with not diseased eyes who may have 1.00D or less of astigmatism.
- Z-1336-2013 — ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact lenses. The Vistakon (galyfilcon A) Contact Lens is indicated for daily wear for the correction of refractive ametropia (myopia and hyperopia) in aphakic or non-aphakic persons with non-diseased eyes who may have 1.00D of astigmatism or less.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Johnson & Johnson Vision Care, Inc.
- K210930 — ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)
- K200243 — ACUVUE (senofilcon A) Soft Contact Lens Multifocal
- K180299 — ACUVUE OASYS (senofilcon A) with Photochromic Additive
- K160212 — ACUVUE (senofilcon C) Soft Contact Lens
- K141670 — ACUVUE (ETAFILCON A) SOFT CONTACT LENS FOR PRESBYOPIA
- K100349 — VISTAKON (NARAFILCON B) CONTACT LENS VISIBILITY TINTED WITH UV BLOCKER
- K073485 — VISTAKON (NARAFILCON) A SOFT CONTACT LENS
- K062614 — VISTAKON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS, CLEAR AND TINTED (VISIBILITY AND/OR COSMETICALLY)
- K051900 — ACUVUE (ETAFILCON A) CONTACT LENS, CLEAR AND WITH VISIBILITY TINT WITH UV BLOCKER, FOR DAILY WEAR
- K032340 — VISTAKON (GALYFILCON A) SOFT CONTACT LENS
- K024177 — ACUVUE 2 COLOURS BRAND (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER
- K010114 — ACUVUE 2 BRAND (ETAFILCON A) CONTACT LENS, WITH UV BLOCKER TINTED (TO MASK OR ENHANCE THE NATURAL IRIS COLOR)
Data sourced from openFDA. This site is unofficial and independent of the FDA.