Facility

JOHNSON & JOHNSON VISION CARE, INC.

7 recall(s) on record — most severe on record: Class II.

Key facts

7recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1000222023
Establishment type	Manufacture Medical Device
Location	7500 Centurion Parkway Jacksonville, FL, US 32256
Registration status	Active · expires 2026
Parent company	Johnson & Johnson Vision Care, Inc. (owner-operator 1024871)

Activity by year

Recalls (7)

Devices registered here (1)

Lenses, Soft Contact, Daily Wear
Product code LPL (opens in a new tab) · Class II · Ophthalmic · 21 CFR 886.5925

Recalls & enforcement

Class IIOngoing2025-06-12
Due to defects (bubbles/voids) identified during standard finished goods testing
Class IITerminated2021-05-06
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
Class IITerminated2019-03-11
One lot of ACUVUE OASYS® for ASTIGMATISM Brand Contact lenses has the potential for a limited number of individual contact lens packages to have an incomplete packaging seal.
Class IITerminated2018-07-23
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.
Class IITerminated2017-12-18
Package integrity failure observed during routine shift package integrity testing at an external re-packager.
Class IITerminated2017-10-19
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Class IITerminated2012-12-21
Limited number of individual contact lens packages may not have been completely sealed.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “JOHNSON & JOHNSON VISION CARE, INC. (FEI 1000222023) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000222023-johnson-johnson-vision-care-inc/

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