Limacorporate recalls

Limacorporate has 16 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 2 Jul 2025. 9 are still ongoing.

Total recalls16since 2015
Last 12 months0reported
Class I00% of total
Ongoing9latest 2 Jul 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 16 100%Class III 0 0%

Why limacorporate is recalled

By year

Ongoing limacorporate recalls

9 active

All limacorporate recalls, newest first

16 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPrima Eccentrical Adaptor With Screw recalled by Limacorporate S.p.ALimacorporateOtherNationwide
DeviceCLASS IIPrima Eccentrical Adaptor With Screw recalled by Limacorporate S.p.ALimacorporateOtherNationwide
DeviceCLASS IITEMA Elbow - Axle Small recalled by Limacorporate S.p.ALimacorporateOtherFL, TX
DeviceCLASS IIPrima TT Glenoid Monoblock/Modular reverse TT baseplates recalledLimacorporatePotency & Assay6 states
DeviceCLASS IIPhysica HPS Tibial Liner #6 H10 recalled by Limacorporate S.p.ALimacorporatePackaging Defects5 states
DeviceCLASS IIREF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate recalledLimacorporatePotency & AssayNationwide
DeviceCLASS IIREF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate recalledLimacorporatePotency & AssayNationwide
DeviceCLASS IISMR TT Hybrid glenoid Std - Peg S recalled by Limacorporate S.p.ALimacorporateOtherMO
DeviceCLASS IITEMA Axle Small recalled by Limacorporate S.p.ALimacorporateOtherTX
DeviceCLASS IIREF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self recalledLimacorporateDevice MalfunctionNationwide
DeviceCLASS IIREF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self recalledLimacorporateDevice MalfunctionNationwide
DeviceCLASS IIDelta Cup Beater  Positioner - Aligner recalled by Limacorporate S.p.ALimacorporateDevice MalfunctionN/A
DeviceCLASS IISMR allen wrench, product recalled by Limacorporate S.p.ALimacorporateOtherN/A
DeviceCLASS IISMR glenosphere impactor/extractor recalled by Limacorporate S.p.ALimacorporateDevice MalfunctionNationwide
DeviceCLASS IISMR Shoulder/Spalla Trial Humeral Head diameter recalledLimacorporatePotency & Assay16 states
DeviceCLASS IISMR Shoulder/Spalla Trial Heads ECC . Adaptor recalledLimacorporatePotency & Assay16 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.