Illuminated Stepped Laser Probe Curved-for use in combination with… — Class II medical device recall Z-2097-2021
Ongoing recall by Dutch Ophthalmic USA, Inc., reported 2021-07-28, distributed nationwide. Barcode label extended expiration date. Barcode located at the short side of the outer box shows 2025-10-27 wh
| Recall number | Z-2097-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dutch Ophthalmic USA, Inc., Exeter, NH, United States |
| Recall initiated | 2021-04-14 |
| Classified | 2021-07-19 |
| Reported by FDA | 2021-07-28 |
| Distributed | Nationwide (US) |
| Quantity | 13 boxes |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 08717872016122 |
| Lot numbers | 039406 |
Product
Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2097-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.