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Recall Observatory FDA recall evidence

Device product

ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.

Z-1476-2024

February 21, 2024

Class II

Product summary

Firm
Abbott Laboratories
Event
Event 94149
Status
Ongoing
Classification
Class II
Quantity
7482 kits
Official record key
device-enforcement:Z-1476-2024

Official wording

Reason: The reason for the recall is the failure of calibration and quality controls due to a manufacturing issue of microparticles not meeting labeled claim. This may lead to incorrect myoglobin results and delayed diagnosis of myocardial infarction.

Code information: LN 2K43-25 - Lot number 50808UN23, exp. 11/30/2024, UDI (01)00380740003302 (17)241130(10)50808UN23; LN 2K43-20 - Lot number 60104UN23, exp. 11/30/2024, UDI (01)00380740003296 (17)241130(10)60104UN23.

Distribution pattern: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, FL, GA, IL, KS, LA, MI, MO, MS, NE, NY, OH, OR, PA, TX, VA, and WI. The countries of Angola, Austria, Belarus, Belgium, Brazil, Czech Republic, France, Germany, Hungary, India, Ireland, Israel, Italy, Japan, Latvia, Lithuania, Luxembourg, Mali, Mexico, Morocco, Poland, Portugal, Peoples Republic of China, Romania, Russia, Saudi Arabia, Slovakia, Slovenia, South Africa, South Korea, Switzerland, Taiwan, Tajikistan, Tanzania, Trinidad & Tobago, Turkey, Uganda, Uruguay, Uzbekistan, and Vietnam.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    failure of calibration and quality controls due to a manufacturing