Official recall record
Maxorb CMC 4" X 4" and 4" X 8"
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-11-15
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Medline has initiated a recall due to defects on pouches that could compromise the device's ability to maintain a sterile barrier. Additionally, patches of burnt or cracked polyethylene have been identified on the inside face of the primary packaging that could also compromise sterility. Recall start date: October 31, 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.