Public recall detail

Erbe Flexible Cryoprobe

2026-02-17

medium
General hospital and personal use Performance
Quick summary

Quick summary: Erbe Flexible Cryoprobe. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-17.

Recommended action

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

Recall details

Quick summary: Erbe Flexible Cryoprobe. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-17.

Official details

Affected product details

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

BrandErbe Elektromedizin Gmbh
ProductErbe Flexible Cryoprobe
IssueMedical devices - Performance
Recall classType I
IdentificationRA-81611

Affected products

ProductErbe Flexible Cryoprobe
LotMore than 10 numbers, contact manufacturer.
Model20402-401
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionErbe Flexible Cryoprobe
ProductErbe Flexible Cryoprobe
LotMore than 10 numbers, contact manufacturer.
Model20402-411
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionErbe Flexible Cryoprobe
ProductErbe Flexible Cryoprobe
LotMore than 10 numbers, contact manufacturer.
Model20402-410
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionErbe Flexible Cryoprobe

Issue

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 you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesErbe Elektromedizin Gmbh Waldhoernlestrasse 17, Tuebingen, Germany, 72072
Recall date2026-02-13
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-81611
Background{}
CompaniesErbe Elektromedizin Gmbh Waldhoernlestrasse 17, Tuebingen, Germany, 72072
AudiencesHealthcare
Source updated2026-02-17

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

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