PlainRecalls

Cordis US Corp

Compiled from official public sources by the publisher.

22 recalls on record · Latest: Apr 9, 2025

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Agency notice ledger

Federal filing book Cordis US Corp MID-BOOK · SINGLE-AGENCY

#730 of 14,151 · 22 notices · 0.021% archive

  • BOOK 22 notices
  • RANK #730 of 14,151
  • SHARE 0.021% archive
  • AGENCY FDA Devices (22)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 9, 2025
  • PHOTO Accuray Incorporated

Nearest notice-volume peer: Accuray Incorporated (0 notice gap)

Cordis US Corp accounts for about 0.021% of the 104,423-notice archive on 22 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 Cordis US Corp sits among 14,151 recalling firms

Cordis US Corp ranks 730th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Cordis US Corp vs all firms by recall-notice count

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

22 730th of 14151 higher than 13,394 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

Cordis US Corp in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Cordis US Corp holds about 0.021% of archive notices alongside 22 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 9, 2025

Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
FDA Devices Moderate Apr 9, 2025

Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only
FDA Devices Moderate Mar 19, 2025

Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
FDA Devices Moderate Jan 17, 2024

MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.
FDA Devices Moderate Jan 17, 2024

MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites
FDA Devices Critical Nov 15, 2023

Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
FDA Devices Moderate Dec 21, 2022

Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
FDA Devices Moderate Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX.

Cordis US Corp 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.

Accuray Incorporated 22 Ge Healthcare Finland Oy 22 Integrated Medical Systems Inc 22 Medicrea International 22

Frequently Asked Questions

How many federal recall notices name Cordis US Corp? ▼
PlainRecalls indexes 22 distinct federal recall events naming Cordis US Corp, 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 Cordis US Corp sit among other recalling firms? ▼
Cordis US Corp ranks #730 of 14,151 by distinct recall-event count among 14,151 firms in this archive (95th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Cordis US Corp's notices? ▼
FDA Devices accounts for 22 of this firm's 22 indexed notices.
What product category dominates Cordis US Corp's filing book? ▼
Filings for Cordis US Corp 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.
Cordis US Corp: 22 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 Cordis US Corp; individual notices remain authoritative on each linked recall page.

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