Home › ESCALON MEDICAL CORP. › Irrigating Contact Lens
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
| Date | Firm | Reason |
|---|---|---|
| 2023-09-26 | B. 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 |
| 2010-05-12 | Insight 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 |
| 2010-05-12 | Insight 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 |
| 2007-04-09 | Oasis Medical Inc | Plastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes. |
| 2007-04-09 | Oasis Medical Inc | Plastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes. |
| 2007-04-09 | Oasis Medical Inc | Plastic shavings are coming from the product handle during irrigation. Use of this product may leave plastic shavings in the patient's eyes. |
| 2007-03-02 | Becton Dickinson and Company | Mislabeled: Carton label incorrectly labeled as Ref 581618 (.40 X 16mm) , may contain product Ref 581617 (.50 x 16mm) |
| 2005-08-24 | Oasis 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 |
| 2005-08-24 | Oasis 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 |
| 2005-08-24 | Oasis 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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
