Comprehensive Shoulder System Primary Mini And Primary Length Shoulder Stem (2017-12-21)
Recall Summary Johnson & Johnson is recalling Comprehensive Shoulder System Primary Mini and Primary Length Shoulder Stem devices used in shoulder replacement surgery across Canada. The recall was issued due to issues with these medical devices. This affects patients who received these shoulder implants.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-05-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9edc63bf-8f97-41d4-b8bd-ec1f6447da2c