SPINEART SA recalls
Every recall we track for SPINEART SA — 13 in all, from 2017–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from SPINEART SA peaked in 2017 (7); 13 since 2017.
All FDA recall records for SPINEART SA since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 4 | 3 | 7 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 2 | 0 | 2 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for SPINEART SA recalls
What to do if you have a recalled SPINEART SA product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All SPINEART SA recalls
6 shown- Lower riskMedical device
SPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S
SPINEART SA recalls PERLA cannulated fenestrated polyaxial screws (model MPF-PS 5:55 45-S) due to potential incorrect labeling. Affected units may have safety risks if mislabeled.
PERLAJun 30, 2025 - Lower riskMedical device
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
Spineart recalls PERLA TL 25D screws with model numbers TLF-DS 45-65 series due to setscrew insertion problems that may cause improper tightening or misalignment.
SpineartMar 15, 2024 - Use cautionMedical device
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,
SPINEART recalls specific JULIET Ti Lateral Lumbar Ti-Life Plate models that may disassemble during surgery, causing delays. Affected patients should contact SPINEART for guidance.
SPINEARTMar 16, 2023 - Lower riskMedical device
SPINEART SA recalls PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle
SPINEART recalls PERLA TL Lateral Connector Open models with incorrect rod size labeling. Affected units may have wrong size labels, potentially causing improper spinal fixation in pediatric cases.
SPINEARTApr 9, 2021 - Lower riskMedical device
SPINEART SA recalls Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
SPINEART recalls JULIET Ti OL cage for orthopedic spinal procedures due to incorrect inner blister pack labeling. This mismatch may cause confusion in surgical use.
SPINEARTFeb 5, 2019 - Lower riskMedical device
SPINEART SA recalls TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM, LENGTH 14 MM, REF TRY-PS-40 14-S, Qty 2 TRYPTIK(R) 2C-Plate
SPINEART recalls TRYPTIK 2C-Plate screws with batch 3-5934 due to incorrect labeling showing a self-drilling screw sketch. This may cause confusion in surgical use. Affected patients should contact SPINEART for guidance.
SPINEARTNov 27, 2017
SPINEART SA recall questions
How many recalls has SPINEART SA had?
13 recalls from SPINEART SA are on record with U.S. safety agencies, from 2017–2025.
What is the most recent SPINEART SA recall?
SPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S, dated Jun 30, 2025. Every SPINEART SA recall is listed on this page, newest first.
Why are SPINEART SA products recalled?
The most common reasons on record: Cannulated fenestrated polyaxial screws may be incorrectly labeled (2).
What should I do if I have a recalled SPINEART SA product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new SPINEART SA recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.