Pulse*Spray® Infusion Systems recall in Canada: Performance issue
In plain language
This recall involves Pulse*Spray® Infusion Systems 3fx135x120 sold in Canada. It's being recalled because a component may have a manufacturing defect affecting its seal. Contact the manufacturer for more information.
What to do
- Contact the manufacturer, Angiodynamics, Inc., for additional information.
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Affected products
Pulse*Spray® Infusion Systems 3fx135x120
Model: 12500415
Lot: 5793480
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: 5793480
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 12500415
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 Pulse*Spray® Infusion Systems 3fx135x120 sold in Canada. It's being recalled because a component may have a manufacturing defect affecting its seal. Contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer, Angiodynamics, Inc., 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 January 5, 2024.
Is the Analytic Technology Corp brand affected by this recall?
Yes, Analytic Technology Corp products are affected by this recall. This recall involves Pulse*Spray® Infusion Systems 3fx135x120 sold in Canada. It's being recalled because a component may have a manufacturing defect affecting its seal. Contact the manufacturer for more information.