Bard Gastric and Esophageal Balloons recall in Canada: Performance issue
In plain language
This recall involves Bard Gastric and Esophageal Balloons sold in Canada. They are being recalled because users may have difficulty removing plastic plugs, potentially damaging the device. This recall is for the healthcare industry.
What to do
- Contact the manufacturer for additional information.
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Affected products
Bard Single Intragastric Linton Balloon Tube
Model: 0092740
Lot: All lots
Bard Blakemore Esophageal-Nasogastric Tube
Model: 0092100, 0092110, 0092300
Lot: All lots
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube
Model: 0092220
Lot: All lots
Why this matters
Performance issue
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 0092100, 0092110, 0092220, 0092300, 0092740
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?
Performance issue
What should consumers do?
Contact the manufacturer for 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. Performance issue
When was this product recalled?
This product was recalled on April 22, 2025.
Is the C.R. Bard, Inc. brand affected by this recall?
Yes, C.R. Bard, Inc. products are affected by this recall. This recall involves Bard Gastric and Esophageal Balloons sold in Canada. They are being recalled because users may have difficulty removing plastic plugs, potentially damaging the device. This recall is for the healthcare industry.