Official recall record
Coloplast Catheters
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-12-30
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
This recall is due to breach in sterility barrier (packaging pouch). The products involved with a sterilization issue was tested to evaluate impact to package integrity (blue-dye penetration test). Pouch integrity failures were observed due to holes in the pouch. This defect is not easily visible by the product's users. Recall start date: December 2, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.