Alaris Pump Module recall in Canada: under or over infusion risk
In plain language
This recall involves the Alaris Pump Module Model 8100 sold in Canada. It's being recalled because a component defect could lead to under or over infusion of medication to a patient. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information on affected lot or serial numbers.
- Follow the manufacturer's instructions for return or repair.
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Affected products
Alaris Pump Module Model 8100
Model: 8100
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Under or 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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8100
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?
Under or over infusion risk
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information on affected lot or serial numbers. Follow the manufacturer's instructions for return or repair.
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. Under or over infusion risk
When was this product recalled?
This product was recalled on May 4, 2018.
Is the Alaris brand affected by this recall?
Yes, Alaris products are affected by this recall. This recall involves the Alaris Pump Module Model 8100 sold in Canada. It's being recalled because a component defect could lead to under or over infusion of medication to a patient. Stop using the product and follow the return steps in the official notice.