ICU Medical Burette Set recall in Canada: performance issue
In plain language
This recall involves the ICU Medical Burette Set (Clave, Shut-Off) sold in Canada. It's being recalled because the tubing connected to the burette component may separate. This recall is intended for the healthcare industry.
What to do
- Contact the manufacturer for additional information.
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Affected products
Burette Set (Clave, Shut-Off)
Model: B9732
Lot: 14149636
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: 14149636
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: B9732
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 the ICU Medical Burette Set (Clave, Shut-Off) sold in Canada. It's being recalled because the tubing connected to the burette component may separate. This recall is intended for the healthcare industry.
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?
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 October 22, 2025.
Is the Icu Medical Inc. brand affected by this recall?
Yes, Icu Medical Inc. products are affected by this recall. This recall involves the ICU Medical Burette Set (Clave, Shut-Off) sold in Canada. It's being recalled because the tubing connected to the burette component may separate. This recall is intended for the healthcare industry.