# FDA recall Z-2097-2021

> **Dutch Ophthalmic USA, Inc.** · Class II · device recall initiated 2021-04-14.

## 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

## Distribution

Nationwide Distribution in the states of CA, FL, MA,  and UT.

## Key facts

- **Recall number:** Z-2097-2021
- **Recalling firm:** Dutch Ophthalmic USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-04-14
- **Report date:** 2021-07-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Exeter, NH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2097-2021

## Citation

> AI Analytics. FDA recall Z-2097-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2097-2021. Source: US FDA. Licensed CC0.

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