FDA recall record

SPINEART SA JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 recall — FDA Z-1426-2023

JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation,…

Class IIclassification
Z-1426-2023official record ID
May 3, 2023report date

Recall record at a glance

Official recordZ-1426-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSPINEART SA
Report dateMay 3, 2023
Recall initiation dateMar 16, 2023
Quantity544
LocationPlan-Les-Ouates, N/A, Switzerland

Official product description

JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT-PL 02 12-S, JLT-PL 02 14-S, JLT-PL 02 16-S; JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE LARGE, REF: JLT-PL 04 08-S, JLT-PL 04 10-S, JLT-PL 04 12-S, JLT-PL 04 14-S, JLT-PL 04 16-S, JLT-PL 04 18-S

Why the product was recalled

JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation, or during surgery when removing the implant holder, which could cause surgical delay.

Distribution information

US Nationwide distribution in the states of NH, TX, CA, VA, IL, RI, NC, AZ.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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