Oridion Medical recall in Canada: Medical device labelling and packaging issue
In plain language
This recall involves various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer, Oridion Medical 1987 Ltd., for additional information.
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Affected products
Filterline Set
Model: XS04620
Lot: All lots.
Filterline H Set Infant/Neonatal
Model: 006324
Lot: All lots.
Omni Ventline Set
Model: 012495
Lot: All lots.
Filterline H Set
Model: XS04624
Lot: All lots.
Filterline H Set Adult/Pediatric
Model: 007737 010580
Lot: All lots.
Airway Adapter, Adult/Pediatric
Model: 010989
Lot: All lots.
CO2 Sampling Line
Model: 010991
Lot: All lots.
Filterline H Set Infant/Neonatal, Long
Model: 007738
Lot: All lots.
Filterline Set Long, Adult/Pediatric
Model: 010579 007768
Lot: All lots.
Vitaline H Set Adult/Pediatric
Model: 010787
Lot: All lots.
Vitaline H Set Infant/Neonatal
Model: 010807
Lot: All lots.
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 006324, 007737 010580, 007738, 010579 007768, 010787, 010807, 010989, 010991, 012495, XS04620, XS04624
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Contact the manufacturer, Oridion Medical 1987 Ltd., for additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on March 6, 2025.
Is the Oridion Medical brand affected by this recall?
Yes, Oridion Medical products are affected by this recall. This recall involves various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.