ARES Catheter recall in Canada: infection risk
In plain language
This recall involves ARES Ventricular Catheters, Peritoneal Catheters, and Catheter Kits sold in Canada. They are being recalled because a defect in the outer pouch seal may compromise sterility. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot or serial numbers if provided.
- Contact Medtronic Inc. for further instructions.
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Affected products
ARES VENTRICULAR CATHETER WITH RIGHT ANGLE CLIP AND STYLE
Model: 91101
Lot: 10265137, 10265138, 10278409, 10297691, 10297693, 10297696, 10353501
ARES PERITONEAL CATHETER
Model: 93092
Lot: 10273893, 10278418, 10312362, 10316961
ARES KIT VENTRICULAR CATHETER WITH RIGHT ANGLE CLIP AND STYLET AND PERITONEAL CATHETER
Model: 95001
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Risk of post-operative infection
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: 10265137, 10265138, 10278409, 10297691, 10297693, 10297696, 10353501, 10273893, 10278418, 10312362, 10316961, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 91101, 93092, 95001
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?
Risk of post-operative infection
What should consumers do?
Stop using the product immediately. Check the lot or serial numbers if provided. Contact Medtronic Inc. for further instructions.
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. Risk of post-operative infection
When was this product recalled?
This product was recalled on December 24, 2020.
Is the ARES brand affected by this recall?
Yes, ARES products are affected by this recall. This recall involves ARES Ventricular Catheters, Peritoneal Catheters, and Catheter Kits sold in Canada. They are being recalled because a defect in the outer pouch seal may compromise sterility. Stop using the product and follow the return steps in the official notice.