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Vista Clean Multi-Purpose Solution

Nomax, Inc. · Model A · UDI-DI 00351801021016

LPN

510(k) clearances

8,017

Adverse events (2 deaths)

Recalls

Facilities

Description

Vista Clean multi-purpose contact lens solution cleans, rinses, disinfects, stores, and conditions contact lenses. Vista Clean is compatible for use with any lens type including RGP lenses, scleral lenses, hybrid lenses, and soft lenses including silicone hydrogel.

Recalls

Date	Firm	Reason
2022-06-23	Family Dollar Stores, Llc.	Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-06-23	Family Dollar Stores, Llc.	Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-06-23	Family Dollar Stores, Llc.	Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-05-25	Mckesson Medical-Surgical Inc. Corporate Office	Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2020-12-29	Allergan PLC	Missing Instruction For Use insert.
2016-09-19	Bausch & Lomb Inc Irb	Product was found to contain excess residual levels of hydrogen peroxide.
2011-02-21	Marietta Vision	Product is misbranded; Product labeled as, Made in the Netherlands, was actually manufactured in Mexico.
2010-07-23	Abbott Medical Optics Inc (AMO)	The recall was initiated after AMO determined, through internal testing, that a limited number of the flip top caps used during production of these solutions may leak and, although
2010-07-23	Abbott Medical Optics Inc (AMO)	The recall was initiated after AMO determined, through internal testing, that a limited number of the flip top caps used during production of these solutions may leak and, although
2009-08-17	Bausch & Lomb Inc	During routine testing the product failed to meet shelf life specifications.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.