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Dutch Ophthalmic USA, Inc.

Dutch Ophthalmic USA, Inc. Recalls

All product recalls associated with Dutch Ophthalmic USA, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Apr 2021

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Dutch Ophthalmic USA, Inc.: Illuminated Stepped Laser Probe Curved-for use in combina...

Barcode label extended expiration date. Barcode located at the short side of the outer box shows 2025-10-27 when scanned, while the correct expiry date is 2024-10-01

FDAApr 14, 2021Nationwide• Dutch Ophthalmic USA, Inc.

Dutch Ophthalmic USA, Inc.: Disposable Replacement Backflush Brush Needles (23 gauge/...

Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label states (20 gauge/0.9 mm) instead of the correct size of 23 gauge/0.6 mm and the correct product code 1281.B1D06

FDAFeb 25, 2021IL, IN, MO +1 more• Dutch Ophthalmic USA, Inc.

Dutch Ophthalmic USA, Inc.: The device is a 25-gauge infusion line that is part of 25...

Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing 23-gauge infusion line

FDA

May 21, 2019

Nationwide

• Dutch Ophthalmic USA, Inc.