PlainRecalls

Creganna Medical Devices

Compiled from official public sources by the publisher.

5 recalls on record · Latest: Aug 9, 2023

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Agency notice ledger

Federal filing book Creganna Medical Devices LIGHT-BOOK · SINGLE-AGENCY

#2,435 of 14,151 · 5 notices · 0.005% archive

  • BOOK 5 notices
  • RANK #2,435 of 14,151
  • SHARE 0.005% archive
  • AGENCY FDA Devices (5)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 9, 2023
  • PHOTO A G Specialty Foods I…

Nearest notice-volume peer: A G Specialty Foods Inc (0 notice gap)

Creganna Medical Devices accounts for about 0.005% of the 104,423-notice archive on 5 distinct filings — a light 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 Creganna Medical Devices compares to 14,151 recalling firms

Creganna Medical Devices ranks 2,435th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Creganna Medical Devices vs all firms by recall-notice count

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

5 2435th of 14151 higher than 11,411 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 · 2026-09-16

Creganna Medical Devices in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Creganna Medical Devices holds about 0.005% of archive notices alongside 5 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 9, 2023

Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access
FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004EPTMCA85400
FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004EPTMCA85300
FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, SYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USMC85100
FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200

Creganna Medical Devices is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name Creganna Medical Devices? ▼
PlainRecalls indexes 5 distinct federal recall events naming Creganna Medical Devices, 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 Creganna Medical Devices sit among other recalling firms? ▼
Creganna Medical Devices ranks #2,435 of 14,151 by distinct recall-event count among 14,151 firms in this archive (81st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Creganna Medical Devices's notices? ▼
FDA Devices accounts for 5 of this firm's 5 indexed notices.
What product category dominates Creganna Medical Devices's filing book? ▼
Filings for Creganna Medical Devices 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.
Creganna Medical Devices: 5 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 Creganna Medical Devices; individual notices remain authoritative on each linked recall page.

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