Quick summary: Exoplan. Reason: Performance. Category: General hospital and personal use. Date: 2026-05-20.
Exoplan
2026-05-20
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Exoplan. Reason: Performance. Category: General hospital and personal use. Date: 2026-05-20.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
During internal testing of libraries an error was identified within specific Straumann surgical protocol libraries used with Exoplan version 3.1. Under certain implant/sleeve/workflow selections, the protocol output displays an incorrect instrument combination in the final drilling steps. In two consecutive protocol steps an incorrect drill key is displayed, which may result in a drilling depth up to 2 mm deeper than intended. This may lead to unintended injury depending on anatomical conditions and clinical use. The deviation is limited to specific implant/sleeve/workflow selections and does not affect all protocol configurations.
What you should do
- DO NOT USE AFFECTED LIBRARY AS PER THE FIELD SAFETY NOTICE.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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