Prismaflex Control Units
In plain language
This recall involves Prismaflex Control Units and associated sets sold in Canada. They are being recalled because the deaeration chamber may dislodge from the control unit. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
Prismaflex ST100 Sets
Model: 107636
Lot: All lots
Oxiris Set Row
Model: 973003
Lot: All lots
Prismaflex HF1000 Set
Model: 107140, PRISMAFLEX HF1000
Lot: All lots
Prismaflex ST150 Set
Model: 107640, PRISMAFLEX ST150 SET
Lot: All lots
Prismaflex TPE 2000 Set
Model: 107144, PRISMAFLEX TPE 2000
Lot: All lots
Why this matters
Medical device performance issue
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: 107140, 107144, 107636, 107640, 973003, PRISMAFLEX HF1000, PRISMAFLEX ST150 SET, PRISMAFLEX TPE 2000
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?
Medical device performance issue
What should consumers do?
Contact the manufacturer 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?
Yes, there may be a health risk. Medical device performance issue
When was this product recalled?
This product was recalled on January 20, 2026.
Is the Vantive Health Gmbh brand affected by this recall?
Yes, Vantive Health Gmbh products are affected by this recall. This recall involves Prismaflex Control Units and associated sets sold in Canada. They are being recalled because the deaeration chamber may dislodge from the control unit. Healthcare professionals should contact the manufacturer for more information.