Johnson & Johnson Vision Care, Inc.: FDA recalls

FDA enforcement reports name Johnson & Johnson Vision Care, Inc. as the recalling firm in 7 events. The events have 10 product records. The recalls started from 2012 to 2025. All the events are device recalls.

See the 7 events

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Enforcement events

7 events, newest first.

FDA enforcement events of Johnson & Johnson Vision Care, Inc.
Initiated	Product (first record)	Type	Class	Records	Status
12 Jun 2025	ACUVUE OASYS MAX 1-Day MULTIFOCAL	Device	Class II	1	Ongoing
6 May 2021	ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50	Device	Class II	1	Terminated
11 Mar 2019	ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.	Device	Class II	1	Terminated
23 Jul 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…	Device	Class II	1	Terminated
18 Dec 2017	ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.	Device	Class II	1	Terminated
19 Oct 2017	ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS	Device	Class II	3	Terminated
21 Dec 2012	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…	Device	Class II	2	Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Follow by RSS:Food, drug and device recallsFDA Class I recalls

Type and class

Johnson & Johnson Vision Care, Inc.: events for each product type
Type		Events
Device		7

Johnson & Johnson Vision Care, Inc.: events in each class
Class		Events
Class II		7

Share of the events of the firm in Class I: 0%
Share of all events on the register in Class I: 18%
Events with the status Ongoing: 1

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Johnson & Johnson Vision Care, Inc., by the year that the recall started. The largest year is 2017, with 2 events.

Official channels

FDA enforcement reportsThe FDA search of the weekly enforcement reports.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA: report a problemThe FDA page that shows where a report about a product goes.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Cite this page

Recall Register. Johnson & Johnson Vision Care, Inc.: FDA recalls. https://recallregister.com/firm/johnson-johnson-vision-care-inc/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
State of the firm address: FL

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Johnson & Johnson Vision Care, Inc. have?: Class II: 7 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Johnson & Johnson Vision Care, Inc.?: FDA event 97095, which the firm started on 12 Jun 2025. The first product in the record is: ACUVUE OASYS MAX 1-Day MULTIFOCAL
How many FDA recalls of Johnson & Johnson Vision Care, Inc. have the status Ongoing?: 1 event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.