CanadaThe TEGO Connector from ICU Medical Inc. (model/catalogue number D 1000) is affected; affected units are identified by lot or serial numbers consisting of more than 10 numbers—contact the manufacturer to confirm. It was recalled because ICU Medical identified lot‑specific issues with the silicone seal on the TEGO device; contact the manufacturer if you require additional information.
What's being recalled
Companies: ICU Medical Inc., 951 Calle Amanecer, San Clemente, California, United States, 92673.
How to identify it
Affected products: TEGO Connector; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: D 1000
The hazard
ICU Medical has identified lot-specific issues with the silicone seal on the TEGO device.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States