Dutch Ophthalmic USA, Inc. recalls

3 recalls on record · latest: April 14, 2021

Official U.S. recall history for Dutch Ophthalmic USA, Inc., compiled from official government records.

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Dutch Ophthalmic USA, Inc. recalls Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC

April 14, 2021 · Medical device recalls Moderate risk Barcode label extended expiration date. Barcode located at the short side of th…

Dutch Ophthalmic USA product recalled over labeling errors

February 25, 2021 · Medical device recalls Moderate risk Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label state…

Dutch Ophthalmic USA, Inc. recalls The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectomy Pack VGPC 25g, P…

May 21, 2019 · Medical device recalls Moderate risk Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing 23-gau…