PlainRecalls

Limacorporate S.p.A

Compiled from official public sources by the publisher.

16 recalls on record · Latest: Jul 2, 2025

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Agency notice ledger

Federal filing book Limacorporate S.p.A LIGHT-BOOK · SINGLE-AGENCY

#977 of 14,151 · 16 notices · 0.015% archive

  • BOOK 16 notices
  • RANK #977 of 14,151
  • SHARE 0.015% archive
  • AGENCY FDA Devices (16)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 2, 2025
  • PHOTO Acella Pharmaceutical…

Nearest notice-volume peer: Acella Pharmaceuticals, LLC (0 notice gap)

Limacorporate S.p.A accounts for about 0.015% of the 104,423-notice archive on 16 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Limacorporate S.p.A sits among 14,151 recalling firms

Limacorporate S.p.A ranks 977th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Limacorporate S.p.A vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

16 977th of 14151 higher than 13,145 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Limacorporate S.p.A in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Limacorporate S.p.A holds about 0.015% of archive notices alongside 16 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 2, 2025

PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
FDA Devices Moderate Jul 2, 2025

PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile
FDA Devices Moderate Jan 1, 2025

TEMA Elbow - Axle Small REF 1590.15.010 TEMA Elbow - Axle Large REF 1590.15.020 TEMA Elbow System is a cemented total elbow prosthesis.
FDA Devices Moderate Jan 24, 2024

PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510, BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810, BASEPLATE D.25MM FULL WEDGED 15-degrees/1975.14.615, BASEPLATE D.28MM FULL WEDGED 15-degrees/1975.14.815, BASEPLATE D.28MM FULL WEDGED 15-degrees X/1975.14.865, BASEPLATE D.25 MM FULL WEDGED 20-degrees/1975.14.620, BASEPLATE

FDA Devices Moderate Dec 20, 2023

PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610
FDA Devices Moderate Jul 5, 2023

REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
FDA Devices Moderate Jul 5, 2023

REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R
FDA Devices Moderate Apr 5, 2023

SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
FDA Devices Moderate Mar 22, 2023

TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)
FDA Devices Moderate Oct 27, 2021

REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852
FDA Devices Moderate Oct 27, 2021

REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE R, 2100099, UDI: (01)08033390018845
FDA Devices Moderate Nov 15, 2017

Delta Cup Beater  Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System
FDA Devices Moderate Sep 7, 2016

SMR allen wrench 5 mm, product code 9013.50.210
FDA Devices Moderate Jun 1, 2016

SMR glenosphere impactor/extractor; Used to implant the glenosphere in the SMR Reverse Shoulder replacement.
FDA Devices Moderate Sep 9, 2015

SMR Shoulder/Spalla Trial Heads ECC .4 mm Adaptor, REF 9013.30.021; SMR Shoulder/Spalla Trial Heads ECC .8 mm Adaptor, REF 9013.30.031; for use in shoulder implant surgery.
FDA Devices Moderate Sep 9, 2015

SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm, REF 9013.22.425; SMR Shoulder/Spalla Trial Humeral Head diameter .44 mm, REF 9013.22.445; SMR Shoulder/Spalla Trial Humeral Head diameter .46 mm, REF 9013.22.465; for use in shoulder implant surgery.

Limacorporate S.p.A holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Cell Marque Corporation 16 Churchill Medical Systems, Inc. 16 Flower Orthopedics Corporation 16 Greatbatch Medical 16

Frequently Asked Questions

How many federal recall notices name Limacorporate S.p.A? ▼
PlainRecalls indexes 16 distinct federal recall events naming Limacorporate S.p.A, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Limacorporate S.p.A sit among other recalling firms? ▼
Limacorporate S.p.A ranks #977 of 14,151 by distinct recall-event count among 14,151 firms in this archive (93rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Limacorporate S.p.A's notices? ▼
FDA Devices accounts for 16 of this firm's 16 indexed notices.
What product category dominates Limacorporate S.p.A's filing book? ▼
Filings for Limacorporate S.p.A span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Limacorporate S.p.A: 16 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Limacorporate S.p.A; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026