Mega 2000™ and Mega Soft™ Patient Return Electrodes - Potential Risk of Patient Burn Injuries
What the notice records
| Product | Mega 2000™ and Mega Soft™ Patient Return Electrodes |
|---|---|
| Issue | Revised instructions for use - Labelling and packaging - Increased risk or new adverse events |
| What you should do | No advice recorded on the notice |
| Category | General hospital and personal use - General and plastic surgery |
| Publishing body | Marketed health products |
| Class | Class not stated |
| Last updated | 2024-07-31 |
Read the official notice on recalls-rappels.canada.ca
Everything in General hospital and personal use - General and plastic surgery · Everything from Marketed health products
Read this correctly
This page reproduces the fields published on the notice and links to the notice itself. It is not a rating and not a statement about a product's current condition, availability or safety.
This notice carries no class in the published data. A blank class means the field is blank — it is not a statement that the product was low risk.
Privacy
This site publishes records that governments already publish. It sets no cookie and makes no request to Google unless you accept one. Read more below.
About this record
Every recall notice published by Health Canada: the product, the issue recorded against it, the class assigned, and the official notice itself. A record of what was published, on the date it was published.
Source: Health Canada — Recalls and safety alerts (open data) — Open Government Licence – Canada. Data refreshes daily. Every page links the row it came from.
What this site is not. It is a copy of an official record. It is not a judgement about any business, building or person, and it is not advice. If the record is wrong, the source above is where it is corrected.