Volk Optical Inc

Complete recall history across all FDA and CPSC categories, 4 total recalls

Volk Optical Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by Volk Optical Inc

Date Product Reason Class
Feb 2, 2016 Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for ... The firm discovered that the incorrect lot number was engraved on the product. Class III
Feb 27, 2015 Lombart 90D Clear with case Visualization during diagnosis and laser therapy... Mislabeling. The incorrect lot number was engraved on the anodized aluminum ... Class III
Feb 27, 2015 Volk 25D Large Clear BIO Lens with case UPC: 8 11608 01010 6, VOLK OPTICAL IN... Mislabeling. The incorrect lot number was engraved on the anodized aluminum ... Class III
Oct 25, 2012 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization ... The defect was with mis-engraving of the lot # directly on the product and it... Class III

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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