Reported May 3, 2023 · Ongoing

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,…

Spineart Sa

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: SPINEART SA · Chemin Du Pre-Fleuri 3 · Plan-Les-Ouates, N/A · N/A

Is this the product you have?

  • 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
Lot codes and dates

11 of 11 products

Products covered by this recall
#BarcodesProduct as published
107640178987388REF/UDI-DI/Lot: JLT-PL 02 08-S/07640178987388/4-8826, 5-4142, 5-5377, 5-0643, 5-2431
207640178987395JLT-PL 02 10-S/07640178987395/6-5488, 6-6556, 5-0644, 6-4734, 6-4735, 5-5378, 6-3211
307640178987401JLT-PL 02 12-S/07640178987401/6-5489, 6-6558, 6-7645, 6-8734, 6-4732, 4-8828, 5-5379, 6-4733
407640178987418JLT-PL 02 14-S/07640178987418/5-8439, 4-8829, 6-0714, 5-5380
507640178987425JLT-PL 02 16-S/07640178987425/4-8830, 5-4145, 6-3217, 6-0726, 6-5490
607640178987456JLT-PL 04 08-S/07640178987456/4-8845, 5-4146, 6-0725
707640178987463JLT-PL 04 10-S/07640178987463/4-8831, 5-4147, 6-0722
807640178987470JLT-PL 04 12-S/07640178987470/4-8832, 5-4148, 5-8438, 6-0721, 6-3209
907640178987487JLT-PL 04 14-S/07640178987487/4-3861, 4-8833, 5-4149
1007640178987494JLT-PL 04 16-S/07640178987494/5-4150
1107640178987500JLT-PL 04 18-S/07640178987500/5-4151
Amount recalled
544

Where it was sold

Why it 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.