PlainRecalls

NeuroLogica Corporation

Compiled from official public sources by the publisher.

13 recalls on record · Latest: Nov 19, 2025

Subscribe to new NeuroLogica Corporation recalls (RSS)

Agency notice ledger

Federal filing book NeuroLogica Corporation LIGHT-BOOK · SINGLE-AGENCY

#1,191 of 14,151 · 13 notices · 0.012% archive

  • BOOK 13 notices
  • RANK #1,191 of 14,151
  • SHARE 0.012% archive
  • AGENCY FDA Devices (13)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 19, 2025
  • PHOTO Access Scientific LLC

Nearest notice-volume peer: Access Scientific LLC (0 notice gap)

NeuroLogica Corporation accounts for about 0.012% of the 104,423-notice archive on 13 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 →

How NeuroLogica Corporation compares to 14,151 recalling firms

NeuroLogica Corporation ranks 1,191st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

NeuroLogica Corporation vs all firms by recall-notice count

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

13 1191st of 14151 higher than 12,927 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

NeuroLogica Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows NeuroLogica Corporation holds about 0.012% of archive notices alongside 13 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 19, 2025

GM85 Digital Mobile X-ray imaging System; Model Number: GM85;
FDA Devices Moderate Aug 28, 2024

GM60A. Digital Diagnostic Mobile X-Ray System.
FDA Devices Moderate Feb 21, 2024

Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
FDA Devices Moderate Jul 12, 2023

OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck Model Number: NL5000
FDA Devices Moderate Apr 26, 2023

Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
FDA Devices Moderate Aug 19, 2020

OmniTom Computed tomography x-ray system, Model NL5000, all NL5000 systems with software version before 05.01.01 - Product Usage: is intended to be used for x-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck.
FDA Devices Moderate Aug 21, 2019

WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07, 3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02, 4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07, 4.01.08, 4.01.09.
FDA Devices Moderate Aug 21, 2019

HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12
FDA Devices Moderate Jun 5, 2019

Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The GM85 Digital X-ray imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications
FDA Devices Moderate Apr 25, 2018

Solid state x-ray imager (flat panel/digital imager) Solid state x-ray imager (flat panel/digital imager) Medical
FDA Devices Moderate Mar 14, 2018

The GC80 Digital X-ray Imaging System
FDA Devices Moderate Sep 6, 2017

Samsung GU60A system- Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications
FDA Devices Moderate Nov 18, 2015

Samsung GM60A-40S Intended for use in generating radiographic images of human anatomy.

NeuroLogica Corporation holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (13 here — thin-book).

Access Scientific LLC 13 Acclarent, Inc. 13 Advanced Bionics, LLC 13 Aequita Pharmacy 13 Alden Optical 13

Similar medical devices volume

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

Access Scientific LLC 13 Acclarent, Inc. 13 Advanced Bionics, LLC 13 Aequita Pharmacy 13

Frequently Asked Questions

How many federal recall notices name NeuroLogica Corporation? ▼
PlainRecalls indexes 13 distinct federal recall events naming NeuroLogica Corporation, 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 NeuroLogica Corporation sit among other recalling firms? ▼
NeuroLogica Corporation ranks #1,191 of 14,151 by distinct recall-event count among 14,151 firms in this archive (91st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of NeuroLogica Corporation's notices? ▼
FDA Devices accounts for 13 of this firm's 13 indexed notices.
What product category dominates NeuroLogica Corporation's filing book? ▼
Filings for NeuroLogica Corporation 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.
NeuroLogica Corporation: 13 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 NeuroLogica Corporation; individual notices remain authoritative on each linked recall page.

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