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LacriPure

MENICON AMERICA, INC. · Model 7P · UDI-DI 00853253003201

LPN
1
510(k) clearances
8,010
Adverse events (2 deaths)
23
Recalls
32
Facilities

Recalls

DateFirmReason
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2020-12-29Allergan PLCMissing Instruction For Use insert.
2016-09-19Bausch & Lomb Inc IrbProduct was found to contain excess residual levels of hydrogen peroxide.
2011-02-21Marietta VisionProduct is misbranded; Product labeled as, Made in the Netherlands, was actually manufactured in Mexico.
2010-07-23Abbott 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
2010-07-23Abbott 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
2009-08-17Bausch & Lomb IncDuring 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.