PlainRecalls

Agfa N.v.

Compiled from official public sources by the publisher.

7 recalls on record · Latest: Sep 4, 2024

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Agency notice ledger

Federal filing book Agfa N.v. LIGHT-BOOK · SINGLE-AGENCY

#1,861 of 14,151 · 7 notices · 0.007% archive

  • BOOK 7 notices
  • RANK #1,861 of 14,151
  • SHARE 0.007% archive
  • AGENCY FDA Devices (7)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 4, 2024
  • PHOTO A I Foods Corporation

Nearest notice-volume peer: A I Foods Corporation (0 notice gap)

Agfa N.v. accounts for about 0.007% of the 104,423-notice archive on 7 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 Agfa N.v. compares to 14,151 recalling firms

Agfa N.v. ranks 1,861st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Agfa N.v. vs all firms by recall-notice count

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

7 1861st of 14151 higher than 12,091 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 · 2026-09-14

Agfa N.v. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Agfa N.v. holds about 0.007% of archive notices alongside 7 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 4, 2024

DR 800. Digital Radiography X-ray System.
FDA Devices Moderate Apr 10, 2024

Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generate projection X-Ray images of human patients. Models: 5411/ 050, A5411/ 0300 and A5411/ 0400
FDA Devices Moderate Jun 10, 2020

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product Usage: DR 800: Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system

FDA Devices Moderate Mar 25, 2020

AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications
FDA Devices Moderate Aug 7, 2019

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following an anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system is intended for projec
FDA Devices Low Mar 27, 2019

PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film REF: XJUB8, XJM73, XJUDD, XJM85, EKLYZ. Product Usage: Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run shows pinholes in different frequencies and intensities.
FDA Devices Moderate Oct 3, 2018

DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton (including skull, spinal column and extremities), chest, abdomen and other body parts on adult, pediatric or neonatal patients.

Agfa N.v. 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.

Abbott Diagnostics Scarborough, Inc. 7 Alto Development Corp 7 Ambu Inc. 7 Andover Healthcare Inc. 7

Frequently Asked Questions

How many federal recall notices name Agfa N.v.? ▼
PlainRecalls indexes 7 distinct federal recall events naming Agfa N.v., 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 Agfa N.v. sit among other recalling firms? ▼
Agfa N.v. ranks #1,861 of 14,151 by distinct recall-event count among 14,151 firms in this archive (85th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Agfa N.v.'s notices? ▼
FDA Devices accounts for 7 of this firm's 7 indexed notices.
What product category dominates Agfa N.v.'s filing book? ▼
Filings for Agfa N.v. 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.
Agfa N.v.: 7 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 Agfa N.v.; individual notices remain authoritative on each linked recall page.

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