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Health Canada Medical devices

Tamper Evident Additive Port Cap

Issued November 13, 2025
Issue
The recall was initiated by IMI following their internal discovery that the corrugated shipper box contains incorrect compatibility information. All other information on the box label is correct, including the device label and IFU. Users are advised to not discard or return the device as it is safe to use, and to verify compatibility using the device label and IFU, not the shipper box.
Hazard description
Labelling and packaging
Product
Product name
Tamper Evident Additive Port Cap
Reference
ID
RA-81213