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Disposable Infusion Cannula, 6.0 mm.

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Model 1272.BD · UDI-DI 08717872002255

KYG Prescription

510(k) clearances

2,134

Adverse events

Recalls

Facilities

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

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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.