Alaris Pump Administration Sets recall in Canada: Medical device issue
In plain language
This recall involves Alaris Pump Administration Sets sold in Canada. They are being recalled because they may not prime correctly, which could affect their function. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model or catalog numbers if provided.
- Contact BD Switzerland SARL for return instructions.
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Affected products
INFUSION SET - SS MF LOW SORBING
Model: 11532269
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - LOW SORB CV SS
Model: 10013072
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - NV SS CHECK VALVE
Model: 10013361, 10013361T
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - LOW SORB NV CV SS BAG ACCESS PORT
Model: 10015861A
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - CV SS
Model: 10013186, 11404930, 11590100
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - DP CKV SS DEHP FREE
Model: 10817613
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV SMS DP
Model: 2421-0500
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV SS DP
Model: 11287205
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV CV SS DEHP FREE
Model: 2420-0007
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV CKV SMS DP
Model: 2420-0500
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV CKV SS DP
Model: 2426-0007, 2426-0500
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV CKV MF SMS
Model: 2430-0500, 2432-0007
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - V/NV MC SS DP DEHP
Model: 10010541, 10010541-07
Lot: More than 10 numbers, contact manufacturer.
INFUSION SET - SMARTSITE
Model: 2452-0007
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Medical device issue affecting function
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10010541, 10010541-07, 10013072, 10013186, 10013361, 10013361T, 10015861A, 10817613, 11287205, 11404930, 11532269, 11590100, 2420-0007, 2420-0500, 2421-0500, 2426-0007, 2426-0500, 2430-0500, 2432-0007, 2452-0007
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?
Medical device issue affecting function
What should consumers do?
Stop using the product immediately. Check the model or catalog numbers if provided. Contact BD Switzerland SARL for return 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. Medical device issue affecting function
When was this product recalled?
This product was recalled on May 11, 2018.
Is the Alaris brand affected by this recall?
Yes, Alaris products are affected by this recall. This recall involves Alaris Pump Administration Sets sold in Canada. They are being recalled because they may not prime correctly, which could affect their function. Stop using the product and follow the return steps in the official notice.