Erbe Flexible Cryoprobe
Brand(s)
Last updated
Summary
Product
Erbe Flexible Cryoprobe
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Erbe Flexible Cryoprobe | More than 10 numbers, contact manufacturer. | 20402-401 |
| Erbe Flexible Cryoprobe | More than 10 numbers, contact manufacturer. | 20402-411 |
| Erbe Flexible Cryoprobe | More than 10 numbers, contact manufacturer. | 20402-410 |
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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
| Erbe Elektromedizin Gmbh |
| Waldhoernlestrasse 17, Tuebingen, Germany, 72072 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-81611
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