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FDA (Device enforcement)Recalled 2026-02-06class ii

BD KIESTRA LAB AUTOMATION: BD Kiestra" ReadA; Catalog No.: 446948.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Domestic: KS, MD, MN, NJ, TX, VA; International: Australia, Austria, Belgium, Canada, China, Denmark, France, Germany, Hong Kong, Italy, Kuwait, Mexico, Morocco, Netherlands, Norway, Saudi Arabia, Spain, Sweden, Switzerland, Taiwan, United Kingdom; Quantity: 82 units (7 US, 65 OUS) Lot/code info: Catalog No.: 446948; UDI-DI: 00382904469481; Serial Numbers: All;

UPC codes

00382904469481

Source

Official record: FDA (Device enforcement)

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

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