HemoCue AB
Complete recall history across all FDA and CPSC categories — 5 total recalls
HemoCue AB 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 (5)
FDA medical device enforcement actions by HemoCue AB
| Date | Product | Reason | Class |
|---|---|---|---|
| May 12, 2025 | The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue G... | Glucose microcuvettes experienced transit time outside of limits, so stabilit... | Class II |
| Jul 25, 2013 | HemoCue¿ Hb 201 Microcuvettes, carton/4 boxes/25 pouches of Microcuvettes, He... | HemoCue AB has become aware of a production related problem involving punctur... | Class II |
| Jul 16, 2013 | HemoCue¿ Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, ... | HemoCue AB has become aware of a production related problem involving punctur... | Class II |
| Jul 15, 2013 | HemoCue¿ Glucose 201 Microcuvettes, 25 Microcuvettes Individually Packaged. ... | During a complaint investigation HemoCue AB discovered punctured HemoCue Gluc... | Class II |
| Nov 7, 2012 | Analyzing system consists of a small and portable analyzer and plastic microc... | Incorrect version of Quick Reference Guide (QRG) was delivered with products ... | 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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