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
Dutch Ophthalmic USA recalls their Illuminated Stepped Laser Probe (Product Code 7510.ALC) because the barcode label shows an expired date (2025-10-27) instead of the correct expiration (2024-10-01). This could lead to using expired equipment, though the hazard is not immediately dangerous.
The barcode label on the outer box shows an expiration date of October 27, 2025, but the correct expiration is October 1, 2024. This mismatch could cause confusion about whether the product is expired, potentially leading to using outdated equipment.
Ophthalmologists and medical facilities using the Illuminated Stepped Laser Probe (Product Code 7510.ALC) with Lot Number 039406. Those most at risk are healthcare professionals handling the product without verifying the expiration date.
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.
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.
The barcode label shows an expiration date of 2025-10-27 instead of the correct 2024-10-01, which could cause confusion about whether the product is expired.
Check for Product Code 7510.ALC, Lot Number 039406, and Unique Device Identifier 08717872016122. The barcode label on the short side of the outer box shows the incorrect expiration date.
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.
We’ve drafted a message you can send Dutch Ophthalmic to request your refund or repair — edit it as you like.
Subject: Recall Z-2097-2021 — Dutch Ophthalmic Dutch Ophthalmic Hello, I own a Dutch Ophthalmic that is covered by recall Z-2097-2021 from Dutch Ophthalmic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
