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.
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
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Contact the company
📍Recalling firmDutch Ophthalmic USA, Inc.10 Continental Dr Bldg 1 · Exeter, NH 03833-7507
“Dutch Ophthalmic Illuminated Stepped Laser Probe: Expired Barcode Label Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62792-dutch-ophthalmic-illuminated-stepped-laser-probe-expired-barcode-label-risk. Based on FDA recall #Z-2097-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2097-2021%22&limit=1).
Dutch Ophthalmic USA, Inc. is recalling Illuminated Stepped Laser Probe Curved products due to barcode labels showing an incorrect expiration date, according to the FDA on April 14, 2021.
How to tell if you have it
Brand: Dutch Ophthalmic
Product Code: 7510.ALC
Lot Number(s): 039406
Unique Device Identifier (UDI): 08717872016122
The hazard
The barcode label displays an extended expiration date of 2025-10-27, while the correct expiry date is 2024-10-01.
Context
GovInfoNow's records show Dutch Ophthalmic USA, Inc. has 2 other recalls on record since 2019-05-21. Other recent recalls of similar products include BD Ready-to-Use Hydrophilic Catheter 14 Fr: Incorrect Expiration Date Labeling (2025-11-29), Inspire Respiratory Sensing Lead Model 4340: Incorrect Use By Date May Cause Unplanned Surgery (2026-05-11), and Expressaire Disposable Tourniquet Cuff Recall: Wrong Expiration Date (2026-08-24).
How to tell if you have this one
Check for the product code 7510.ALC on the box. Look for Lot Number 039406 and the Unique Device Identifier 08717872016122. The barcode label on the short side of the outer box shows the incorrect expiration date.
Brand
Dutch Ophthalmic
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Verify Expiration Date
Check the barcode label on the short side of the outer box for the expiration date. If it shows 2025-10-27 instead of 2024-10-01, the product is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Nationwide Distribution in the states of CA, FL, MA, and UT.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Massachusetts, Utah.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
No, the recall does not require stopping use. The issue is a labeling error that may cause confusion about expiration, but it does not pose an immediate safety risk.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2097-2021 (April 14, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2097-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.