Volk Optical Inc: Medical Device Recall in 2015 - (Recall #: Z-2055-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.

Product Classification:

Class III

Date Initiated: February 27, 2015

Date Posted: July 15, 2015

Recall Number: Z-2055-2015

Event ID: 71048

Reason for Recall:

Mislabeling. The incorrect lot number was engraved on the anodized aluminum ring. The correct lot number is BE03356; however, BD03356 was engraved on the ring in error.

Status: Terminated

Product Quantity: 78 units

Code Information:

Model: L90C, Lot: BE03356,

Distribution Pattern:

Distribution to VA only

Voluntary or Mandated:

Voluntary: Firm initiated