Reported Jul 28, 2021 · Ongoing
Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC
Dutch Ophthalmic USA, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Dutch Ophthalmic USA, Inc. · 10 Continental Dr Bldg 1 · Exeter, NH · 03833-7507
Is this the product you have?
- Illuminated Stepped Laser Probe Curved-for use in combination
- with 23G vitrectomy system Product Code7510.ALC
- Lot codes and dates
- Lot Number(s) 039406 Unique Device Identifier (UDI) 08717872016122
- Amount recalled
- 13 Boxes
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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