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Irrigating Contact Lens

ESCALON MEDICAL CORP. · Model Flat · UDI-DI 00853480006136

KYG Prescription
1
510(k) clearances
2,140
Adverse events
11
Recalls
82
Facilities

Description

For use during silicone oil procedures, irrigating contact lens enables visualization of surgical field while ensuring proper irrigation of cornea and orbit. Single -use requiring no clean up.

Recalls

DateFirmReason
2023-09-26B. Braun Medical, Inc.Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and heal
2010-05-12Insight Instruments, Inc.Insight Instruments, Inc., Stuart, FL is recalling CORNEA COAT 2.5% Hydroxypropylmethylcellulose solution in 1.5 ml Syringe due to a potential weakness of the peel pouch seals. Pr
2010-05-12Insight Instruments, Inc.Insight Instruments, Inc., Stuart, FL is recalling CORNEA COAT 2.5% Hydroxypropylmethylcellulose solution in 1.5 ml Syringe due to a potential weakness of the peel pouch seals. P
2007-04-09Oasis Medical IncPlastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes.
2007-04-09Oasis Medical IncPlastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes.
2007-04-09Oasis Medical IncPlastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes.
2007-03-02Becton Dickinson and CompanyMislabeled: Carton label incorrectly labeled as Ref 581618 (.40 X 16mm) , may contain product Ref 581617 (.50 x 16mm)
2005-08-24Oasis Medical Inc"Please be aware that this is not a new recall. This recall was initially classified in 2005 (Z-1595-05). The firm has taken action; but, due to administrative issues this product
2005-08-24Oasis Medical Inc"Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues additional products are now being classified by the agency". Foreign de
2005-08-24Oasis Medical Inc"Please be aware that this is not a new recall. This recall was initially classified in 2005 (Z-1595-05). The firm has taken action; but, due to administrative issues this product

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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.