Baxter Intravenous Solution Bags recall in Canada: potential leak
In plain language
This recall involves Baxter Intravenous Solution Bags, including 0.4% Lidocaine & 5% Dextrose Injection, 0.9% Sodium Chloride Injection, Lactated Ringer’s Injection, and Metronidazole Injection, sold in Canada. They are being recalled because they have the potential to leak when the administration port is spiked. Stop using the product if you observe any damage or leakage and consult your healthcare professional.
What to do
- Stop using the product immediately if you see damage or fluid leakage.
- Consult your healthcare professional if you have used an affected lot or have concerns.
- Wear gloves when handling the bag to avoid exposure to any medications.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Potential for delay in therapy, exposure to medication, or infection
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Potential for delay in therapy, exposure to medication, or infection
What should consumers do?
Stop using the product immediately if you see damage or fluid leakage. Consult your healthcare professional if you have used an affected lot or have concerns. Wear gloves when handling the bag to avoid exposure to any medications.
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. Potential for delay in therapy, exposure to medication, or infection
When was this product recalled?
This product was recalled on October 6, 2023.
Is the Baxter brand affected by this recall?
Yes, Baxter products are affected by this recall. This recall involves Baxter Intravenous Solution Bags, including 0.4% Lidocaine & 5% Dextrose Injection, 0.9% Sodium Chloride Injection, Lactated Ringer’s Injection, and Metronidazole Injection, sold in Canada. They are being recalled because they have the potential to leak when the administration port is spiked. Stop using the product if you observe any damage or leakage and consult your healthcare professional.