Every recall we track for Limacorporate S.p.A — 12 in all — plus the complaints and injury reports the public filed about them.
Limacorporate recalls sterile PRIMA 2MM eccentric adaptors with screw (ref 1367.15.702) due to potential missing screw. Affected units have lot number 2416658 or UDI 08033390201827.
Limacorporate recalls sterile PRIMA 4MM eccentric adaptors with missing black laser markings that could cause misalignment during medical procedures.
Limacorporate recalls TEMA Elbow - Axle Small and Large models due to potential mechanical mismatch during revision surgery. Affected units have specific UDI-DI codes and lot numbers.
Limacorporate recalls PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610 due to incorrect product labeling. Affected units include specific lot numbers and serial codes.
Limacorporate recalls specific PRIMA TT Glenoid Monoblock baseplates with potential for loosening due to manufacturing defects. Affected models include D.25mm and D.28mm versions with various wedge angles. Consumers should check product codes and contact Limacorporate for details.
Limacorporate S.p.A recalls Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R) due to potential peripheral holes being out of specification. All lots are affected.
Limacorporate S.p.A recalls Prima TT Genoid Modular Reverse TT Baseplate (Sterile R) due to potential peripheral holes being out of specification. All lots are affected.
Limacorporate recalls SMR TT Hybrid glenoid implants without tantalum markers. Without markers, doctors may misjudge implant position during X-rays, risking improper joint alignment.
Limacorporate recalls TEMA Axle Small (REF 1590.15.010) due to an unapproved component in its elbow prosthesis. Affected users should contact the manufacturer for details.
Limacorporate recalls bone screws that may not match label length. This could lead to improper use in medical procedures. Affected units have specific model numbers and were sold in certain regions.
Limacorporate recalls bone screws that may not match label length. This could lead to improper use during medical procedures. Affected units have specific model numbers and were sold in the U.S. Learn how to check and what to do.
