Recall Atlas
Drugs & medicalClass II

BD KIESTRA LAB AUTOMATION recalls 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…

Read the official notice →
Date
2026-04-08
Country
United States
Brand
BD KIESTRA LAB AUTOMATION
Product
BD Kiestra" ReadA; Catalog No.: 446948.
Classification
Class II
Units
Domestic: KS, MD, MN, NJ, TX, VA; International: Australia, Austria, Belgium,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

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  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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