Health & Personal Care
HIGH
FDA DEVICE
MicroPort Recalls HIPTURN Fem Head Trial Device Over FDA Violation
Due to products not having FDA Premarket authorization to be distributed within the United States.
MicroPort Orthopedics
Due to
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MicroPort Orthopedics Recalls
1 recall found for MicroPort Orthopedics. Check current safety alerts and related brands before using affected products.
- Active recalls
- 1
- Pages
- 1
Brand Statistics
Total Recalls
1
Pages
1