Revitan Modular Revision Hip Systems (2017-01-20)
Revitan Modular Revision Hip Systems Recall Revitan Modular Revision Hip Systems, which are artificial hip replacement components, are being recalled across Canada. The recall was issued due to concerns with the medical device itself, classified as a Class I recall, which indicates a serious issue. This recall affects hip replacement patients who received these systems.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-02-01
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a4c69cc2-5068-4daa-8f7d-6b3e8e5b81e0