Dutch Ophthalmic USA, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2097-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 14, 2021

Date Posted: July 28, 2021

Recall Number: Z-2097-2021

Event ID: 88146

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

Status: Ongoing

Product Quantity: 13 Boxes

Code Information:

Lot Number(s) 039406 Unique Device Identifier (UDI) 08717872016122

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated