Medication Cassette Reservoir recall in Canada: medication leakage
In plain language
This recall involves certain CADD Medication Cassette Reservoirs sold in Canada. They are being recalled because a weakened weld joint could cause medication to leak. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Medication Cassette Reservoir
Model: 21-7001-24, 21-7002-24, 21-7300-24, 21-7301-24, 21-7302-24
Lot: More than 40 numbers, contact manufacturer.
Why this matters
Medication leakage
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 40 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 21-7001-24, 21-7002-24, 21-7300-24, 21-7301-24, 21-7302-24
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?
Medication leakage
What should consumers do?
Contact the manufacturer if you require 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?
Yes, there may be a health risk. Medication leakage
When was this product recalled?
This product was recalled on July 19, 2024.
Is the Smiths Medical Asd Inc. brand affected by this recall?
Yes, Smiths Medical Asd Inc. products are affected by this recall. This recall involves certain CADD Medication Cassette Reservoirs sold in Canada. They are being recalled because a weakened weld joint could cause medication to leak. Healthcare professionals should contact the manufacturer for more information.