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FDA (Device enforcement)Recalled 2024-02-07class ii

Siemens Healthcare Diagnostics, Inc.: DCA Systems HbA1c Reagent Kit

Hazard

The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was confirmed to display a positive bias without alerting the user. The potential impact of the defect is that erroneous test results could be reported and potentially lead to incorrect patient management of glucose control. A positive bias may be observed with eleven HbA1c affected lots. Positive bias was observed when the performance of these five HbA1c lots was compared to NGSP pooled patient target-value assigned samples and the maximum bias observed was 19%.

Details from the source

Reason for recall: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was confirmed to display a positive bias without alerting the user. The potential impact of the defect is that erroneous test results could be reported and potentially lead to incorrect patient management of glucose control. A positive bias may be observed with eleven HbA1c affected lots. Positive bias was observed when the performance of these five HbA1c lots was compared to NGSP pooled patient target-value assigned samples and the maximum bias observed was 19%. Distribution: Worldwide distribution - US Nationwide and the country of Taiwan. Quantity: 74,211 Kits (Expanded 2/28/24: additional 72,892 kits) Lot/code info: Siemens Material Number: 10311134; UDI/DI: 00630414532806; Lot#: 9640093, 0645103, 0648103, 0649103, 0654103 . Expanded Lots (02/28/2024): 0637093, 0641093, 0642093, 0647103, 0653103, 0655103;

UPC codes

00630414532806

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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