PlainRecalls

Carefusion 2200 Inc

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 Dec 14, 2022

Carefusion V. Mueller" SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP INSULATED, OVERALL LENGTH 7-3/4" (195MM), REF F-1003

FDA Devices Moderate Dec 14, 2022

Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP, STRAIGHT OVERALL LENGTH 4" (100MM), REF F-3000

FDA Devices Moderate Dec 14, 2022

Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP, 0.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-1030

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5022

FDA Devices Moderate Dec 14, 2022

Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 7-1/2" (190MM), REF F-1301

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5016

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.5MM TIP, STRAIGHT STANDARD, 8-3/4" (225MM), REF F-5124

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 0.5MM TIP, ANGLED-UP, FINE OVERALL LENGTH 8-3/4" (225MM), REF F-5304

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE, 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5302

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM) , REF F-5128

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069

FDA Devices Moderate Dec 14, 2022

CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5002

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 8" (20.3CM) DEEP STERRAD COMPATIBLE, REF CD2-8ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD3-5ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD2-6ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS QTR-LENGTH CONTAINER 12 X 8" (30.3X20.3CM) 4" (10.2CM) DEEP STERRAD COMPATIBLE, REF CD0-4ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS SMALL CONTAINER 21 X 7" (53.3 X 17.8CM) 5-1/2" (14CM) DEEP STERRAD COMPATIBLE, REF CD4-5ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD1-4ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS MINI CONTAINER 10-1/2 X 7-1/2" (26.7X19.0CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD0-3ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD2-4ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD2-5ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD1-6ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS LARGE, CONTAINER 28 X 11" (71.1 X 27.9CM) 6" (15.2CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-61ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD1-5ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-3ST

FDA Devices Moderate Nov 23, 2022

CareFusion V.Mueller GENESIS SMALL, SHALLOW CONT. 21 X 7" (53.3 X 17.8CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD4-3ST

FDA Devices Moderate Apr 6, 2022

(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Storz Scope, Catalog #88-9808; and (d) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Wolf Scope, Catalog #88-9809.

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Thora-Para 5 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 6 Fr Catheter Drainage Tray w/o Lidocaine

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 8 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis PLUS 6 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 6 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Thora-Para 8 Fr Catheter Drainage Tray

FDA Devices Moderate Jul 29, 2020

Safe-T 5 Fr Thora-Para Tray With 5 Fr. Catheter and Sharps Injury Protection - Drug Free

FDA Devices Moderate Jul 29, 2020

Safe-T 8 Fr Thora-Para Tray With 8 Fr. Catheter and Sharps Injury Protection - Drug Free

FDA Devices Moderate Jul 29, 2020

Thora-Para 5 Fr Non-Valved Catheter Drainage Tray

FDA Devices Moderate Jun 24, 2020

Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.

FDA Devices Moderate Apr 25, 2018

JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X 70MM DISP]; STERILE;

FDA Devices Moderate Apr 25, 2018

Thoracentesis/ Paracentesis Kit 10/CS; STERILE;

FDA Devices Moderate Apr 25, 2018

JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;

FDA Devices Moderate Apr 25, 2018

ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;

FDA Devices Moderate Apr 25, 2018

JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 4, d.) 8G x 6, e.) 11G x 6]; STERILE;

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).

Similar medical devices volume

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

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