Official recall record
Kiestra ReadA
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-18
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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