Dutch Ophthalmic USA, Inc. recalls Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC

Recalled July 28, 2021 · FDA recall Z-2097-2021 · Dutch Ophthalmic USA

Hazard

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 · FDA Class II

Units

13 Boxes

Sold at

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

Description

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

Product

Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC

Manufacturer(s)

Dutch Ophthalmic USA, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →