Graphic Controls Acquisition Corporation

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

Graphic Controls Acquisition Corporation 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 Graphic Controls Acquisition Corporation

Date Product Reason Class
Mar 15, 2022 CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... Class II
Mar 15, 2022 CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... Class II
Mar 15, 2022 CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... Class II
Mar 15, 2022 CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... Class II
Mar 15, 2022 CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779 50602-US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... Class II
Mar 15, 2022 CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US Instructions for Use (IFU) (Instructions for Use) indicate compliance with AN... 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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