SPINEART SA: Medical Device Recall in 2019 - (Recall #: Z-0546-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures

Product Classification:

Class III

Date Initiated: February 5, 2019

Date Posted: December 4, 2019

Recall Number: Z-0546-2020

Event ID: 84219

Reason for Recall:

Inner blister pack label is incorrect and does not match the correct external box label.

Status: Terminated

Product Quantity: 14 pieces distribtued to 1 US Distributor

Code Information:

Model Number: JUT-OX 28 09-S Lot Number: 4-2899 UDI: (01) 0 7640178 97398 5 (11) 181102 (17) 261101 (10) 4-2899

Distribution Pattern:

US: CA OUS: Unknowns

Voluntary or Mandated:

Voluntary: Firm initiated