Official recall record
Adaptor 3602, Connector For Hilger Neurostim Dual
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-10-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Adapter #3602 is being recalled due to potential mechanical instability between adapter #3602 and probe #3602-00-TE when used with the Hilger Facial Nerve Stimulator, leading to physical detachment and potential loss of electrical contact during nerve monitoring.
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 2026-10-15.
Record last checked against the registry on 2026-10-15.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.