REDDY-SAPROPTERIN recall in Canada: Decreased potency
In plain language
This recall involves REDDY-SAPROPTERIN 100mg powder for solution sold in Canada. It's being recalled because of a potential for color change and decreased potency. Consult your healthcare provider before stopping use and follow the instructions in the official notice.
What to do
- Consult your healthcare provider prior to discontinuing use.
- Contact the recalling firm with any questions.
- Report any health product related side effects to Health Canada.
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Affected products
REDDY-SAPROPTERIN Powder for Solution
Lot: T2304679
Why this matters
Decreased potency
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: T2304679
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?
Decreased potency
What should consumers do?
Consult your healthcare provider prior to discontinuing use. Contact the recalling firm with any questions. Report any health product related side effects to Health Canada.
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. Decreased potency
When was this product recalled?
This product was recalled on May 3, 2024.
Is the REDDY-SAPROPTERIN brand affected by this recall?
Yes, REDDY-SAPROPTERIN products are affected by this recall. This recall involves REDDY-SAPROPTERIN 100mg powder for solution sold in Canada. It's being recalled because of a potential for color change and decreased potency. Consult your healthcare provider before stopping use and follow the instructions in the official notice.