FDA Device Intelligence
Home › D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. › Reusable universal cannula.(20 gauge / 0.9 mm)

Reusable universal cannula.(20 gauge / 0.9 mm)

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Model 1272.CRPP1 · UDI-DI 08717872002309

NGY Prescription
1
510(k) clearances
346
Adverse events
11
Recalls
61
Facilities

Recalls

DateFirmReason
2025-08-05Alcon Research LLCDue to incomplete seals in the pouch which provide the sterile barrier.
2023-02-20Mani, Inc. - Kiyohara FacilityA packaging defect may compromise the sterile barrier.
2020-10-27Mani, Inc. - Kiyohara FacilityDimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
2020-10-27Mani, Inc. - Kiyohara FacilityDimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
2015-08-11Alcon Research, Ltd.The product has potential to leak beyond their design specification.
2015-08-11Alcon Research, Ltd.The product has potential to leak beyond their design specification.
2015-08-11Alcon Research, Ltd.The product has potential to leak beyond their design specification.
2012-05-29Alcon Research, LTD.This medical device correction is related to Alcon products that present a 23G non-valved trocar cannula and infusion cannula together because of an issue regarding the loose fit b
2009-04-29Alcon Laboratories, IncSpecific lots of Alcon 25 GA Trocar Blades do not conform to finished product specifications in that oxidation can occur on some of the blades.
2009-04-29Alcon Laboratories, IncSpecific lots of Alcon 25 GA Trocar Blades do not conform to finished product specifications in that oxidation can occur on some of the blades.

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 docs
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.