Ga Health Company Limited

Complete recall history across all FDA and CPSC categories — 11 total recalls

Ga Health Company Limited 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 (11)

FDA medical device enforcement actions by Ga Health Company Limited

Date Product Reason Class
Nov 3, 2020 STOPCON Disposable Valves Set-Single Use Valves (suction-/air-water-/biopsy... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 STOPCON Suction Valve-Suction Valve for GI-Endoscope DISTRIBUTED BY: KEY SUR... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 STOPCON Disposable Valves Set-Single Use Single Use Valves Olympus R (Air-... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 ScopeValet Guardian Disposable Endoscope Valves Set- Air/Water, Suction, Bio... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 Bulldog Disposable Endoscope Valves Set-Air/Water Valve, Suction Valve, Biops... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 Bulldog Disposable Endoscope Valves Set-Air/Water Valve, Suction Valve,Biopsy... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 Andorate Disposable Endoscope Valves Set-Contains Suction, Air/Water, Biopsy ... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 Andorate Disposable Endoscope Valves Set-Contains Air/Water Valve,Suction Val... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 STOPCON Disposable Endoscope Valves Set-Single Use Valves Olympus R (Air-Wa... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 Andorate Disposable Endoscope Valves Set-5-piece Valve, Connector and Cleanin... Suction button is reported sticky and/or broken during or after the procedure... Class II
Nov 3, 2020 ScopeValet Guardian Disposable Endoscope Valves Set Distributed By Ruhof Corp... Suction button is reported sticky and/or broken during or after the procedure... 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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