Every recall we track for SPINEART SA — 13 in all — plus the complaints and injury reports the public filed about them.
SPINEART SA recalls PERLA cannulated fenestrated polyaxial screws (model MPF-PS 6:45 40-S) due to possible incorrect labeling. Affected units may have wrong specifications.
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.
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.
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.
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.
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.
SPINEART recalls TRYPTIK 2 C-Plate self-tapping screws due to incorrect labeling that may confuse with self-drilling screws. Affected products have a specific reference code and batch number.
SPINEART recalls TRYPTIK 2C-Plate screws with incorrect labeling that may show a self-drilling screw sketch instead of intended design. Affected units include specific model and batch numbers.
SPINEART recalls TRYPTIK 2C-Plate screws with incorrect labeling that may show a self-drilling screw sketch. Affected products include specific model and batch numbers. Consumers should check their items and contact SPINEART for details.
SPINEART recalls TRYPTIK 2 C-Plate self-tapping screws with incorrect labeling that may confuse with self-drilling screws. Affected units have a specific reference code and batch number.
SPINEART recalls TRYPTIK 2C-Plate self-tapping screws with incorrect labeling that may show a self-drilling screw sketch instead of intended design. Affected units include specific batch numbers for spinal surgery implants.
SPINEART recalls TRYPTIK 2 C-Plate self-tapping screws with incorrect labeling that may show a self-drilling screw sketch. This could lead to improper use in spinal surgery. Affected units include specific model and batch numbers.
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.
