Official recall record
Fassier-Duval Telescopic IM System (FRT250 - 4.0-6.4 Cartridge)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-07-22
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
It has been identified that an incorrect sub-component, FRT240-HEX, was used in place of the FRT250-HEX during assembly. If such an FRT250 cartridge is used in surgery, it will not function correctly for the retrieval of the Fassier-Duval female component. Recall Start Date: July 4, 2024
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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