Limacorporate S.p.A recalls
Every recall we track for Limacorporate S.p.A — 12 in all, from 2017–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Limacorporate S.p.A peaked in 2023 (6); 12 since 2017.
All FDA recall records for Limacorporate S.p.A 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 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 5 | 1 | 6 |
| 2024 | 0 | 0 | 0 | 1 | 1 |
| 2025 | 0 | 0 | 1 | 1 | 2 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Limacorporate S.p.A 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 Limacorporate S.p.A recalls
9 shown- Lower riskMedical device
Limacorporate S.p.A recalls PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
Limacorporate recalls sterile PRIMA 4MM eccentric adaptors with missing black laser markings that could cause misalignment during medical procedures.
Limacorpor: S.p.AMay 19, 2025 - UnratedMedical device
Limacorporate S.p.A recalls TEMA Elbow - Axle Small REF 1590.15.010 TEMA Elbow - Axle Large REF 1590.15.020 TEMA Elbow System is a cemented total
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.
LimacorporateOct 2, 2024 - Lower riskMedical device
Limacorporate S.p.A recalls PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610
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.
LimacorporateOct 27, 2023 - Lower riskMedical device
Limacorporate S.p.A recalls PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM
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.
LimacorporateAug 29, 2023 - Lower riskMedical device
Limacorporate S.p.A recalls REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
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.
Limacorpor: S.p.AMay 30, 2023 - Lower riskMedical device
Limacorporate S.p.A recalls SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
Limacorporate recalls SMR TT Hybrid glenoid implants without tantalum markers. Without markers, doctors may misjudge implant position during X-rays, risking improper joint alignment.
LimacorporateFeb 21, 2023 - UnratedMedical device
Limacorporate S.p.A recalls TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)
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.
LimacorporateJan 25, 2023 - Lower riskMedical device
Limacorporate S.p.A recalls REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI:
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.
LimacorporateOct 1, 2021 - Lower riskMedical device
Limacorporate S.p.A recalls Delta Cup Beater Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System
Limacorporate recalls Delta Cup Beater Positioner model 9057.20.555 used in hip implants due to potential weakness from suboptimal welding. Affected units include specific lot numbers sold in 2014-2016.
LimacorporateSep 8, 2017
Limacorporate S.p.A recall questions
How many recalls has Limacorporate S.p.A had?
12 recalls from Limacorporate S.p.A are on record with U.S. safety agencies, from 2017–2025.
What is the most recent Limacorporate S.p.A recall?
Limacorporate S.p.A recalls PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile, dated May 19, 2025. Every Limacorporate S.p.A recall is listed on this page, newest first.
What should I do if I have a recalled Limacorporate S.p.A 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 Limacorporate S.p.A 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.