PlainRecalls

Carefusion 2200 Inc

Compiled from official public sources by the publisher.

112 recalls on record · Latest: Aug 23, 2023

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Agency notice ledger

Federal filing book Carefusion 2200 Inc HEAVY-BOOK · MULTI-AGENCY

#147 of 14,151 · 112 notices · 0.107% archive

  • BOOK 112 notices
  • RANK #147 of 14,151
  • SHARE 0.107% archive
  • AGENCY FDA Devices (110)
  • CAT medical devices
  • CATS 2 categories
  • LATEST Aug 23, 2023
  • PHOTO Steris Corporation

Nearest notice-volume peer: Steris Corporation (0 notice gap)

Carefusion 2200 Inc accounts for about 0.107% of the 104,423-notice archive on 112 distinct filings — a heavy 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 Carefusion 2200 Inc sits among 14,151 recalling firms

Carefusion 2200 Inc ranks 147th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Carefusion 2200 Inc vs all firms by recall-notice count

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

112 147th of 14151 higher than 14,003 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 2200 Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Carefusion 2200 Inc holds about 0.107% of archive notices alongside 112 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 112 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

FDA Devices Moderate Apr 25, 2018

Manometer, 550 ml three-Way Stopcock; STERILE;
FDA Devices Moderate Sep 28, 2016

Broselow/Hinkle, PEDIATRIC EMERGENCY SYSTEM, PINK/RED Oxygen Delivery Module 2/PACK, Product Code 7700RAW2
FDA Devices Moderate Sep 28, 2016

Broselow/Hinkle, PEDIATRIC EMERGENCY SYSTEM, Broselow Complete Set of Colored Pouches, Product Code 7730MOD
FDA Devices Critical Aug 3, 2016

DIAMOND-FLEX CIRCULAR RETRACTOR, ANGLED, 40MM 5MM, Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date Code: C16. Designed to retract or elevate organs and tissue to provide better visualization access.
FDA Devices Moderate Oct 1, 2014

CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.
FDA Drug Moderate Jun 11, 2014

CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-013-15.
FDA Drug Moderate Jun 11, 2014

CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-003-18
FDA Devices Moderate Sep 18, 2013

*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL 60085 USA; *** 2) Cat. 4341BSDF; Qty. 10; Safe-T Thoracentesis Tray; With Catheter and Sharps Injury Protection; Drug Free; CareFusion; 1500 Waukegan Road; McGaw Park, IL 60085 USA. Indicated for specimen retrieval and therapeutic drainage of the pleural cavity.
FDA Devices Moderate Aug 21, 2013

1) Adult Manual Resuscitator, 2K8004, Oxygen Reservoir Bag, Adult Mask; 2) Adult Manual Resuscitator, 2K8005, 40" (1.0 m) Oxygen Reservoir Tubing, Adult Mask; 3) Adult Manual Resuscitator, 2K8017, Variable Volume Oxygen Reservoir Tubing, Adult Mask; 4) Adult Manual Resuscitator, 2K8034, 40" (1.0 m) Oxygen Reservoir Tubing, PEEP Valve, without Mask; 5) Adult Manual Resuscitator, 2K8035, Oxygen Reservoir Bag, PEEP Valve, Adult Mask; 6) Pediatric Manual Resuscitator, 2K8037, 40" (1.0 m) O
FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector; an Rx device for single patient use; 30 connectors per box; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.
FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an Rx device for single patient use; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.
FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Heated; an Rx device for single patient use; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.

Carefusion 2200 Inc carries an outsized archive share

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 (112 here — heavy-book).

Steris Corporation 112 Aomori Olympus Co., Ltd. 113 Herbal Doctor Remedies 113 Rabbit Creek Products Inc. 114 Mitsubishi 115

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

Steris Corporation 112 Aomori Olympus Co., Ltd. 113 Raysearch Laboratories Ab 115 Stryker Corporation 115

Frequently Asked Questions

How many federal recall notices name Carefusion 2200 Inc? ▼
PlainRecalls indexes 112 distinct federal recall events naming Carefusion 2200 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 2200 Inc sit among other recalling firms? ▼
Carefusion 2200 Inc ranks #147 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Carefusion 2200 Inc's notices? ▼
FDA Devices accounts for 110 of this firm's 112 indexed notices across 2 issuing agencies.
What product category dominates Carefusion 2200 Inc's filing book? ▼
Filings for Carefusion 2200 Inc span 2 product categories, 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 2200 Inc: 112 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 2200 Inc; individual notices remain authoritative on each linked recall page.

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