· Published by Health Canada · Official notice
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Tamper Evident Additive Port Cap | 58203 | 21-01 |
| Tamper Evident Additive Port Cap | 58590 | 21-01 |
| Tamper Evident Additive Port Cap | 57325 | 21-01 |
| Tamper Evident Additive Port Cap | 56586 | 21-01 |
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.