Imactis
Complete recall history across all FDA and CPSC categories — 3 total recalls
Imactis 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 (3)
FDA medical device enforcement actions by Imactis
| Date | Product | Reason | Class |
|---|---|---|---|
| Feb 11, 2021 | Impactis NaviKit-stereotaxic accessory for Computed Tomography systems Ref... | Defect in the mechanical assembly of the needle holder contained in the navig... | Class II |
| Aug 24, 2020 | Imactis Patient Fiducial (Patient Referential), REF: IHR-YY-XXX component ... | The firm has received reports concerning the patient fiducial disk separating... | Class II |
| Aug 1, 2019 | Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref. A10010 ... | The firm has become aware that the sensor cover, a component of the single-us... | 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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