Public recall detail

Kiestra ReadA

2026-02-18

medium
General hospital and personal use Performance
Quick summary

Quick summary: Kiestra ReadA. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-18.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Kiestra ReadA. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-18.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBd Kiestra B.V.
ProductKiestra ReadA
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81617

Affected products

ProductKiestra ReadA
LotMore than 10 numbers, contact manufacturer.
Model446948
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionKiestra ReadA

Issue

BD is currently investigating an issue that can affect remote connectivity between the BD Kiestra™ ReadA modules (discovered through complaints). In some cases, customers have experienced modules becoming unreachable after a reboot, which can lead to delays in plate retrieval from the incubator.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesBD Kiestra B.V. Marconilaan 6, Drachten, Netherlands, 9207 JC
Recall date2026-02-06
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81617
Background{}
CompaniesBD Kiestra B.V. Marconilaan 6, Drachten, Netherlands, 9207 JC
AudiencesHealthcare
Source updated2026-02-18

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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