PlainRecalls

CareFusion 203, Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Oct 1, 2014

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Agency notice ledger

Federal filing book CareFusion 203, Inc. LIGHT-BOOK · SINGLE-AGENCY

#4,540 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,540 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Oct 1, 2014
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company, of St. Paul, Minn. (0 notice gap)

CareFusion 203, Inc. accounts for about 0.002% of the 104,423-notice archive on 2 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 CareFusion 203, Inc. compares to 14,151 recalling firms

CareFusion 203, Inc. ranks 4,540th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

CareFusion 203, Inc. vs all firms by recall-notice count

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

2 4540th of 14151 higher than 8,037 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

CareFusion 203, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows CareFusion 203, Inc. holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Oct 1, 2014

CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum of 5 kg (11 lbs.). It is suitable for service in hospital, transport and homecare as a source of continuous or intermittent positive pressure ventilator support, delivered invasively or non-invasively. These ventilators are restricted medical devices intended for operation by a trained personnel under the direction of a
FDA Devices Critical Jul 25, 2012

CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum of 5 kg (11 lbs). It is suitable for service in hospital and transport environments as a source of continuous or intermittent positive pressure ventilatory support, delivered invasively or non-invasively. It is not intended for homecare use.

CareFusion 203, Inc. 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 CareFusion 203, Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming CareFusion 203, Inc., 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 CareFusion 203, Inc. sit among other recalling firms? ▼
CareFusion 203, Inc. ranks #4,540 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of CareFusion 203, Inc.'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates CareFusion 203, Inc.'s filing book? ▼
Filings for CareFusion 203, Inc. 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.
CareFusion 203, Inc.: 2 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 CareFusion 203, Inc.; individual notices remain authoritative on each linked recall page.

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