Recalls / —
—#183514
Product
Siemens epoc BGEM Test Card-In vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood in the laboratory or at the point of care SMN#/Model #: 10736382
- FDA product code
- CGA — Glucose Oxidase, Glucose
- Device class
- Class 2
- Medical specialty
- Clinical Chemistry
- 510(k) numbers
- K200107
- Affected lot / code info
- Lot Number: 01-20095-10
Why it was recalled
Sporadically inconsistent discrepant (low bias) glucose results on card lot 01-20095-10. Potential exists for a delay in diagnosis of hyperglycemia or unnecessary treatment for hypoglycemia.
Root cause (FDA determination)
Process control
Action the firm took
Siemens issued Urgent Medical Device Correction letter on August 28, 2020 via Federal Express stating the reason for recall communication letter informs customers of the issue and, health risk and action take: Please dispose any inventory of test card lot 01-20095-10 currently in your possession in accordance with local and state disposal requirements. You may request free of charge replacement product from your local Siemens or distributor office. Please review your inventory of these products and assess your laboratorys replacement needs. Please use epoc BGEM Test Card from another unaffected lot. Complete and return the Field Correction Effectiveness Check and Product Replacement Form attached to this letter. Please retain this letter with your laboratory records and forward it to those who may have received this product. Questions, please contact your Siemens Customer Care Center or your local Siemens technical support representative.
Recalling firm
- Firm
- Siemens Healthcare Diagnostics Inc
- Address
- 2 Edgewater Dr, Norwood, Massachusetts 02062-4637
Distribution
- Distribution pattern
- Nationwide Foreign: Canada
Timeline
- Recall initiated
- 2020-08-28
- Terminated
- 2021-09-09
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #183514. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.