Official recall record
Erbe Flexible Cryoprobe
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-17
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Erbe Elektromedizin Gmbh has been made aware of cases of Erbe Flexible Cryoprobes rupturing/bursting during activation. Serious injuries have occurred or could occur due to the failure mode associated with this removal action. Users should stop to use products out of affected lots and follow Erbe's instructions as provided in the field safety notice.
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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