Dutch Ophthalmic USA, Inc. recalls
Every recall we track for Dutch Ophthalmic USA, Inc. — 3 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Dutch Ophthalmic USA, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Dutch Ophthalmic USA, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Dutch Ophthalmic USA, Inc. recalls
3 shown- Lower riskMedical device
Dutch Ophthalmic USA, Inc. recalls Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC
Dutch Ophthalmic USA recalls Illuminated Stepped Laser Probe (Product Code 7510.ALC) due to barcode expiration date showing 2025 instead of 2024. This may cause confusion in product expiration tracking.
Dutch OphthalmicApr 14, 2021 - Lower riskMedical device
Dutch Ophthalmic USA, Inc. recalls Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in vitreoretinal surgery Product Number:
Dutch Ophthalmic USA recalls 23-gauge backflush brush needles labeled as 20-gauge. Mislabeled needles could cause surgical errors. Check product code 1281.B1D06 for affected items.
Dutch OphthalmicFeb 25, 2021 - Lower riskMedical device
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 ,
Dutch Ophthalmic USA recalls 25-gauge surgical packs containing 23-gauge infusion lines. This mismatch risks incorrect surgical use. Affected units have specific product numbers and lot codes.
Dutch OphthalmicMay 21, 2019
Dutch Ophthalmic USA, Inc. recall questions
How many recalls has Dutch Ophthalmic USA, Inc. had?
3 recalls from Dutch Ophthalmic USA, Inc. are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Dutch Ophthalmic USA, Inc. recall?
Dutch Ophthalmic USA, Inc. recalls Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC, dated Apr 14, 2021. Every Dutch Ophthalmic USA, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Dutch Ophthalmic USA, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Dutch Ophthalmic USA, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.