BD KIESTRA LAB AUTOMATION Recalls

1 recall found for BD KIESTRA LAB AUTOMATION. Check if any of your products are affected.

HIGH
FDA DEVICE

BD Kiestra" ReadA; Catalog No.: 446948.

In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the incubator while connectivity was restored. This issue was intermittent and did not affect test results, performance of the assay, or sample integrity.

BD KIESTRA LAB AUTOMATION
In certain
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Brand Statistics

Total Recalls
1
Pages
1