Volk Optical Recalls
4 recalls on record · March 27, 2013 to March 23, 2016 · Medical Devices
Recalls by year
13
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 23, 2016Medical DevicesFDA
Volk Optical Inc recalls Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye ex
Hazard: The firm discovered that the incorrect lot number was engraved on the product.
July 15, 2015Medical DevicesFDA
Volk Optical Inc recalls Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit
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.
June 3, 2015Medical DevicesFDA
Volk Optical Inc recalls Volk 25D Large Clear BIO Lens with case UPC: 8 11608 01010 6, VOLK OPTICAL INC. The Volk Optical BIO Lenses are intende
Hazard: Mislabeling. The incorrect lot number was engraved on the anodized aluminum ring.
March 27, 2013Medical DevicesFDA
Volk Optical Inc recalls 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the h
Hazard: The defect was with mis-engraving of the lot # directly on the product and its packaging. Mixed up device engraving of V20LC (lot # BB09213) with that from V60C (lot # BB09205).