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Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy

Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy Recalls

All product recalls associated with Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 601–620 of 4099 recalls

PRIMA TT Glenoid Baseplate (Limacorporate) – manufacturing hole issue (2023)

Potential for baseplate peripheral holes to be out of specification due to a manufacturing issue, which could lead to loosening of the implant, or the screw moving from its original position.

FDAAug 29, 2023CA, IL, IN +3 more• Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy

Multichem IA Plus (Techno-Path) – glass vial commodity problem (2023)

Laceration Risk

Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem IA Plus and Multichem P Controls. Some customers have experienced broken vials when receiving or thawing Technopath Multichem IA Plus and Multichem S Plus Controls. Breakages have been observed upon delivery, while thawing or while opening the vial. The breakages can result in the bottom of the vial breaking off, breakage in the neck thread area or cracking on the sides of the vial. This may expose the user to biohazardous material if cut and may cause a delay in patient results.

FDAAug 25, 2023Nationwide• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

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Multichem S Plus (Techno-Path) – glass vial commodity problem (2023)

Laceration Risk

FDAAug 25, 2023Nationwide• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

Multichem P (Techno-Path) – glass vial commodity problem (2023)

Laceration Risk

FDAAug 25, 2023Nationwide• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

House Bed Frames (Zipadee Kids) – Entrapment Risk (2023)

This recall involves Zipadee Montessori beds sold in twin, full, and queen size variations of the "Convertible House Bed Frame" and "Montessori Floor Bed." They were shipped between February 26, 2018 and October 22, 2021. Zipadee also sold toddler-size Montessori beds which were manufactured between May and September 2018. The beds are all natural wood floor beds that can be raised or converted to adjust for a child's sleeping needs as they grow and develop. The beds are intended for children 18 months and older.

CPSCAug 17, 2023Nationwide• Bell Station Interiors, dba Zipadee Kids, of Circleville, Ohio

Functional MR Software (Olea Medical) – Export Error (2023)

When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file contents and associated series descriptions to not match, which could lead to a misinterpretation of clinical data.

FDAAug 10, 2023MA, MI• OLEA MEDICAL 93 AVANUE DU SORBIER, ZONE ATHELIA IV LA CIOTAT France

Veran Percutaneous Biopsy Kit (Olympus) – Navigation System Issue (2023)

Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic Navigation System, SPiN Planning Laptop Workstation, and all associated navigation instruments) manufacturing to design requirements and insufficient evidence to demonstrate adequate electromagnetic compatibility (EMC). EMC is the ability of electrical equipment and systems to function acceptably without interference and to not interfere with other devices within its operating environment

FDAAug 10, 2023Nationwide• Olympus Corporation of the Americas

Veran Endobronchial Needle (Olympus) – Navigation System Problem (2023)

FDAAug 10, 2023Nationwide• Olympus Corporation of the Americas

Veran Thoracic Navigation System (Olympus) – Device Nonconformance (2023)

FDAAug 10, 2023Nationwide• Olympus Corporation of the Americas

Veran Percutaneous Track Device (Olympus) – Navigation System Nonconformance (2023)

FDAAug 10, 2023Nationwide• Olympus Corporation of the Americas

Veran Endobronchial Access Catheter (Olympus) – Navigation System Problem (2023)

FDAAug 10, 2023Nationwide• Olympus Corporation of the Americas

Room & Board Crib Mattresses (Restwell) – suffocation hazard (2023)

This recall involves Room & Board brand crib mattresses, Natural Organic Latex and Spring Crib (Model no. 847564) and Natural Organic Latex Crib (Model No. 925869). The crib mattresses are 52 inches long and 28 inches wide, have a white top and gray sides with "Room & Board" embroidered on one end with the model name underneath.

CPSCAug 10, 2023Nationwide• Restwell Mattress Co., of Eden Prairie, Minnesota

Prucka 3 Amplifiers (GE Medical) – Power Supply Failure (2023)

A diode on the power supply of the Prucka 3 Amplifier used with CardioLab/ComboLab systems could reach elevated temperatures and fail, then power off and become inoperable.

FDAAug 8, 2023CA, CO, FL +14 more• GE Medical Systems Information Technologies Inc

Pluvicto (Advanced Accelerator) – Incorrect Labeling (2023)

Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date

Class IIILow

FDAAug 7, 2023Nationwide• Advanced Accelerator Applications USA, Inc.

Liquid Assayed Chemistry Control (Randox) – instructions error (2023)

there has been a transcription error in the Instructions for Use (IFU) for the Liquid Assayed Chemistry Control Premium Plus Level 3. For Caeruloplasmin, the one and two standard deviation values printed on the sheet are incorrect, which may lead to misreporting patient results. Target and range values are correct, and risk is mitigated; most clinical labs will use the target and range values in clinical practice.

FDAAug 3, 2023GA, OH, OR +3 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Salad Kit (NatureBest) – Deer feces contamination (2023)

Potential presence of deer fecal matter.

Class IIModerate

FDAAug 2, 2023TX• NatureBest Pre-Cut & Produce LLc

EVIS EXERA III Duodenovideoscope (Olympus) – infection risk (2023)

Recent reports of patient infection.

FDAJul 27, 2023Nationwide• Olympus Corporation of the Americas

Sprinter (CREATIVE MOBILE) – recreational vehicle problem (2023)

Fire/Burn Risk

Airstream, Inc. (Airstream) is recalling certain 2019-2023 Ford Transit, 2020 RAM, and 2020-2022 Sprinter recreational vehicles upfitted by Creative Mobile Interiors. The fuel hose between the inline fuel filter and the injection pump module (IMP) may have inadequate clamp force, possibly resulting in a gasoline leak.

NHTSAJul 27, 2023Nationwide• CREATIVE MOBILE INTERIORS

Airway Mobilescope (Olympus) – endoscope lodging risk (2023)

Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

FDAJul 27, 2023Nationwide• Olympus Corporation of the Americas

Tracheal Intubation Fiberscope (Olympus) – endoscope lodging risk (2023)

Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

FDAJul 27, 2023Nationwide• Olympus Corporation of the Americas