PlainRecalls

Carefusion 2200 Inc

83 recalls on record · Latest: Aug 23, 2023

Carefusion 2200 Inc Recall Insight

Carefusion 2200 Inc appears on 83 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.099% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Aug 23, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 33 entries, severity tagging shows 4 critical, 29 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 33 of 33 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 2 distinct product categories, with issuing agencies dominated by FDA Devices (31), FDA Drug (2). The date window on this page runs from Jul 11, 2012 to Nov 23, 2022.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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 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 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 Sep 28, 2016

Broselow/Hinkle, PEDIATRIC EMERGENCY SYSTEM, PINK/RED Oxygen Delivery Module 2/PACK, Product Code 7700RAW2

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 ret…

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…

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 …

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, …

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 Parkw…

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, …

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Carefusion 2200 Inc with FORD →

Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds