HemoCue AB: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: January 9, 2013. Most recent: July 9, 2025.

Risk classification: Class II: 4 · Class III: 1

Most recent recalls

DateAgencyProduct
July 9, 2025FDAThe HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (…Z-2070-2025
November 6, 2013FDAHemoCue¿ Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, Sweden Th…Z-0086-2014
November 6, 2013FDAHemoCue¿ Hb 201 Microcuvettes, carton/4 boxes/25 pouches of Microcuvettes, HemoCue AB Ang…Z-0101-2014
September 18, 2013FDAHemoCue¿ Glucose 201 Microcuvettes, 25 Microcuvettes Individually Packaged. The Hemo…Z-2190-2013
January 9, 2013FDAAnalyzing system consists of a small and portable analyzer and plastic microcuvettes. The…Z-0619-2013

Questions about this company

How many recalls does HemoCue AB have?
Recalert has 5 U.S. recalls on record for HemoCue AB, published between January 9, 2013 and July 9, 2025.
What was the most recent HemoCue AB recall?
FDA recall Z-2070-2025, published July 9, 2025: The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (or DM) Analyzer with plasma conversion that multiplies the measured whole blood glucose value by a factor of 1…
Which agencies have handled HemoCue AB recalls?
HemoCue AB appears as the recalling firm in recalls from: FDA (5).

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