FDAFDA · Food and drugs·Recall number Z-1888-2020
Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
Published May 13, 2020 · Recall initiated: April 7, 2020
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The FlexLab Centrifuge Module loading algorithm may lead to unbalanced loads which could damage the centrifuge.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Inpeco S.A.
- Distributor
- Worldwide distribution including the following states: Ohio, New York, Virginia, Pennsylvania, Texas, Delaware, California, Florida, Kentucky, Tennessee, Maryland, Rhode Island, Alabama, Massachusetts, Connecticut, Minnesota, Alabama, Montana, Louisiana, New Jersey, Virginia, New Hampshire, Michigan, North Carolina, Washington, Iowa, New Mexico, Nebraska, and Missouri
- Lot
- Serial Numbers: ACP.357, ACP.388, ACP.396, ACP.397, ACP.399, ACP.400, ACP.402, ACP.404, ACP.405, ACP.407, ACP.408, ACP.409, ACP.410, ACP.412, ACP.413, ACP.416, ACP.417, ACP.418, ACP.419, ACP.420, ACP.421, ACP.422, ACP.423
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Switzerland
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