PlainRecalls

Vygon U.S.A.

Compiled from official public sources by the publisher.

11 recalls on record · Latest: Jun 9, 2021

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Agency notice ledger

Federal filing book Vygon U.S.A. LIGHT-BOOK · SINGLE-AGENCY

#1,410 of 14,151 · 11 notices · 0.011% archive

  • BOOK 11 notices
  • RANK #1,410 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (11)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 9, 2021
  • PHOTO Agfa Corp.

Nearest notice-volume peer: Agfa Corp. (0 notice gap)

Vygon U.S.A. accounts for about 0.011% of the 104,423-notice archive on 11 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 Vygon U.S.A. sits among 14,151 recalling firms

Vygon U.S.A. ranks 1,410th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Vygon U.S.A. vs all firms by recall-notice count

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

11 1410th of 14151 higher than 12,735 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 · 2026-09-15

Vygon U.S.A. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Vygon U.S.A. holds about 0.011% of archive notices alongside 11 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 9, 2021

Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change kit, Product Code: AMS-8465CS.
FDA Devices Moderate Apr 17, 2019

Vygon DUALSTOP Red Cap used for intravascular lines Product Code: 9888.00 - Product Usage: Cap used for intravascular lines.
FDA Devices Moderate Apr 17, 2019

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.
FDA Devices Moderate May 16, 2018

PICC Tray, Product Code: AMS-9093CP Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

PICC Insertion Tray, Product Code: AMS-7192CS-4 Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

Maximum Barrier Insertion Tray, Product Code: AMS-9152CP Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

Maximum Barrier Tray, Product Code: AMS-9018CP Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

Maximum Barrier Tray, Product Code: MCITX-1 Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

PICC Insertion Tray, Product Code: AMS-7192CS-3 Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

Neonatal PICC Tray, Product Code: AMS-8010CP-1 Convenience kit for the insertion of PICCs into the vascular system.
FDA Devices Moderate May 16, 2018

PICC Kit, Product Code: AMS-7063-1 Convenience kit for the insertion of PICCs into the vascular system.

Vygon U.S.A. 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 (11 here — thin-book).

Agfa Corp. 11 Ajinomoto Foods North America Inc. 11 Akron Pharma, Inc. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11

Similar medical devices volume

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

Agfa Corp. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11 Arjohuntleigh Polska Sp. z.o.o. 11

Frequently Asked Questions

How many federal recall notices name Vygon U.S.A.? ▼
PlainRecalls indexes 11 distinct federal recall events naming Vygon U.S.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 Vygon U.S.A. sit among other recalling firms? ▼
Vygon U.S.A. ranks #1,410 of 14,151 by distinct recall-event count among 14,151 firms in this archive (90th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Vygon U.S.A.'s notices? ▼
FDA Devices accounts for 11 of this firm's 11 indexed notices.
What product category dominates Vygon U.S.A.'s filing book? ▼
Filings for Vygon U.S.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.
Vygon U.S.A.: 11 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 Vygon U.S.A.; individual notices remain authoritative on each linked recall page.

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