Every recall we track for MicroPort Orthopedics Inc. — 10 in all — plus the complaints and injury reports the public filed about them.
MicroPort recalls HIPTURN Fem Head Trial 36mm (HTHT003: no FDA premarket approval for US distribution. Affected units sold in the US must stop use immediately.
MicroPort Orthopedics recalls specific knee implant components due to potential incorrect packaging. Affected items may have wrong labeling, but no injury reports. Consumers should check model numbers and contact for details.
MicroPort recalls Evolution MP total knee implants for cemented use only after one incident found with wrong part in packaging. Affected units include specific lot numbers and sizes.
MicroPort Orthoped: Recall of left knee tibial bases (size 2+) with wrong base in packaging. One confirmed incident of incorrect base mix-up during surgery. Affected units: Lot 1916559, REF ETPKN2PL.
MicroPort Orthoped: Size 7 left knee tibial bases (lot 1916715) were recalled due to incorrect product packaging during surgery. Affected patients should contact the manufacturer for details.
MicroPort Orthopedics recalls Profemur Plasma Z Classic Stem Size 7 with missing plasma-spray coating. This could lead to improper fixation in hip replacements. Affected units have specific catalog and lot numbers.
MicroPort Orthopedics recalls specific hip prosthesis models due to reported fractures of titanium modular neck components after implantation. The recall covers 680 fractures globally among 123,840 units sold since 2002.
MicroPort Orthopedics recalls PROFEMUR Neck Long Titanium hip implants (catalog numbers PHA01204-01264) due to reported fractures after implantation. 680 fractures occurred globally among 123,840 implants since 2002.
MicroPort Orthopedics Inc. is a leading manufacturer of medical devices, specializing in orthopedic implants and surgical instruments. They provide high-quality products for various orthopedic procedures.
