Zplp Distal Lateral Fibular Plate
Recall Summary The ZPLP Distal Lateral Fibular Plate, an orthopedic device used in bone surgery, is being recalled in Canada due to performance issues. This recall affects all units of this product distributed across Canada. The device is classified as a Class I recall, the most serious category.
- Product
- ZPLP Distal Lateral Fibular Plate
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-04-08
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d9f7f5ea-9d9e-4a4d-85f0-5e1327899dd3