SPINEART SA recalls Intersomatic JULIET Ti OL cage. For use in orthopedic spinal
Recalled Product
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Hazard / Issue
Inner blister pack label is incorrect and does not match the correct external box label.
Issued by
FDA
Affected States: CA
Lot/Code Info: Model Number: JUT-OX 28 09-S Lot Number: 4-2899 UDI: (01) 0 7640178 97398 5 (11) 181102 (17) 261101 (10) 4-2899
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime