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Volk Optical Inc recalls Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit
Recalled July 15, 2015 · FDA recall Z-2055-2015 · Volk Optical
Hazard
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. · FDA Class III
Units
78 units
Sold at
Distribution to VA only
Description
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.
Product
Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.
Manufacturer(s)
Volk Optical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →