Infusion Sets recall in Canada: over infusion risk
In plain language
This recall involves various Infusion Sets and a Blood Set sold in Canada. They are being recalled because a defect in the pumping segment could lead to over infusion. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot or serial numbers provided in the official notice.
- Contact BD Switzerland SARL for further instructions.
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Affected products
Blood Set - NV, SmartSite Needle-Free Valve Port, Filter
Model: 2477-0000, 2477-0007
Lot: 18015339, 18115199, 18115200, 18116521, 18116637, 18116638, 18116751, 18116752
Infusion Set - SS MF Low Sorbing
Model: 10010453, 10010454
Lot: 17087410, 17087411, 18096003, 18096166, 18096167, 18096235, 18096236, 18096294, 18096295, 18096301, 19026173
Infusion Set - Low Sorb CV SS
Model: 10015414
Lot: 17087329, 17087331, 18036906, 18096654, 18115223
Infusion Set - CV SS
Model: 11404930
Lot: 19025787
Infusion Set - V/NV DP
Model: 2200-0500
Lot: 17087336
Infusion Set - V/NV CV SS DEHP Free
Model: 2420-0007
Lot: 17077398, 18015267, 18015459, 18036965, 18075715, 18076779, 18093077, 18115088, 18115135, 18116500, 18116622, 18116623, 18116624, 19013154, 19013155, 19023000
Infusion Set - V/NV CKV SMS DP
Model: 2420-0500
Lot: 17077358, 18093056, 18116640, 18116641, 18116703
Infusion Set - V/NV CKV SS DP
Model: 2426-0007, 2426-0500
Lot: 17087341, 17125017, 18037029, 18115003, 18115004, 18115006, 18115007, 18115129, 18115132, 18116575, 18116635, 18116647, 18116648, 18116657, 18116658, 19013152, 19013153, 19023005
Why this matters
Over infusion risk
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: 17077358, 18093056, 18116640, 18116641, 18116703, 17077398, 18015267, 18015459, 18036965, 18075715, 18076779, 18093077, 18115088, 18115135, 18116500, 18116622, 18116623, 18116624, 19013154, 19013155, 19023000, 17087329, 17087331, 18036906, 18096654, 18115223, 17087336, 17087341, 17125017, 18037029, 18115003, 18115004, 18115006, 18115007, 18115129, 18115132, 18116575, 18116635, 18116647, 18116648, 18116657, 18116658, 19013152, 19013153, 19023005, 17087410, 17087411, 18096003, 18096166, 18096167, 18096235, 18096236, 18096294, 18096295, 18096301, 19026173, 18015339, 18115199, 18115200, 18116521, 18116637, 18116638, 18116751, 18116752, 19025787
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10010453, 10010454, 10015414, 11404930, 2200-0500, 2420-0007, 2420-0500, 2426-0007, 2426-0500, 2477-0000, 2477-0007
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?
Over infusion risk
What should consumers do?
Stop using the product immediately. Check the lot or serial numbers provided in the official notice. Contact BD Switzerland SARL for further instructions.
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. Over infusion risk
When was this product recalled?
This product was recalled on May 16, 2019.