Olympus Scientific Solutions Americas

Complete recall history across all FDA and CPSC categories — 6 total recalls

Olympus Scientific Solutions Americas 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 (6)

FDA medical device enforcement actions by Olympus Scientific Solutions Americas

Date Product Reason Class
Jul 11, 2017 Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analy... Instruments may, under certain specific circumstances listed below, fail to s... Class II
Jan 7, 2017 Olympus Scientific Solutions Americas Corporation (OSSA) VANTA¿ XRF Analyz... It was discovered under rare circumstances the LED warning light circuit coul... Class II
Oct 27, 2016 Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analy... Possible unintentional x-ray emission after users attempt early termination o... Class II
Jun 22, 2016 Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical ... Trigger lock option does not always prevent x-ray generation. Specifically i... Class II
Jan 13, 2016 Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF Analyzer... The Firm has discovered a Software bug. Class II
Jun 9, 2015 Olympus Scientific Solutions Americas Analytical X-ray System. Delta, Delta... Higher than published scatter around the probe head when testing some samples... Class II

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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