Spineart recalls
3 official recalls and safety alerts involving Spineart since 2023-05, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Spineart or the relevant agency.
- 2025-08-20
USSPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not…
Cannulated fenestrated polyaxial screws may be incorrectly labeled
FDA · DeviceSPINEART SAUS Nationwide distribution in the states of Florida , Kentucky, California.Official notice →- 2024-05-15
- US
SPINEART SA recalls PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S TLF-DS 55 35-S TLF-DS 55…
Due to receiving information regarding difficulties with the insertion of a setscrew inside a screw head. Issues involved, either: 1. The setscrew is not tightened to torque 2. The setscrew is tightened to torque but…
FDA · DeviceSPINEART SAU.S. Nationwide distribution in the states of CA, and KY. Not provided due to…Official notice → - 2023-05-03
- US
SPINEART SA recalls 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 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…
FDA · DeviceSPINEART SAUS Nationwide distribution in the states of NH, TX, CA, VA, IL, RI, NC, AZ.Official notice →