Dutch Ophthalmic USA recalls

Dutch Ophthalmic USA has 3 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 18 Aug 2021. 2 are still ongoing.

Total recalls3since 2021

Last 12 months0reported

Class I00% of total

Ongoing2latest 18 Aug 2021

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why dutch ophthalmic usa is recalled

Other Reasons267%
Labeling Errors133%

Product types

By year

20213100%

Ongoing dutch ophthalmic usa recalls

2 active

Reported	Class	Recall	Company	Reason	Where
18 Aug 2021Device	CLASS II	The device is a 25-gauge infusion line that is part recalled	Dutch Ophthalmic USA	Other	Nationwide
28 Jul 2021Device	CLASS II	Illuminated Stepped Laser Probe Curved-for use recalled	Dutch Ophthalmic USA	Other	Nationwide

All dutch ophthalmic usa recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
18 Aug 2021Device	CLASS II	The device is a 25-gauge infusion line that is part recalled	Dutch Ophthalmic USA	Other	Nationwide
28 Jul 2021Device	CLASS II	Illuminated Stepped Laser Probe Curved-for use recalled	Dutch Ophthalmic USA	Other	Nationwide
28 Jul 2021Device	CLASS II	Disposable Replacement Backflush Brush Needles (/-for use recalled	Dutch Ophthalmic USA	Labeling Errors	4 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.