PlainRecalls

Cardinal Health 200, LLC

194 recalls on record · Latest: Feb 4, 2026

Cardinal Health 200, LLC Recall Insight

Cardinal Health 200, LLC appears on 194 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.231% 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 Feb 4, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 49 of 50 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 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Jul 31, 2019 to Jul 28, 2021.

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 Jul 28, 2021

Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at the point of care by sque…

FDA Devices Moderate Jul 14, 2021

Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442N - Product Usage: intended to be used as protective p…

FDA Devices Moderate Jul 14, 2021

Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442 - Product Usage: intended to be used as protective patient cover…

FDA Devices Moderate Jul 14, 2021

Sterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525 - Product Usage: intended to be used as protective patient coverings, such …

FDA Devices Moderate Jul 14, 2021

Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, s…

FDA Devices Moderate Jul 14, 2021

Nonsterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525N - Product Usage: intended to be used as protective patient coverings, s…

FDA Devices Moderate Jul 14, 2021

Nonsterile Radial/Femoral Angiography Drape, Catalog Number 29529N - Product Usage: intended to be used as protective patient coverings, such as to i…

FDA Devices Moderate Jul 14, 2021

Sterile Femoral Angiography Drape, Catalog Numbers: a) 29460, b) 29456 - Product Usage: intended to be used as protective patient coverings, such as…

FDA Devices Moderate Apr 14, 2021

Enteral Infusion Pump

FDA Devices Moderate Mar 31, 2021

In-View Clear Leggings Sterile

FDA Devices Moderate Mar 24, 2021

JUDKINS PACK

FDA Devices Moderate Mar 24, 2021

McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of…

FDA Devices Moderate Mar 24, 2021

Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdr…

FDA Devices Moderate Feb 17, 2021

Lab Coats SMS X-Large Blue, SKU 2203LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protec…

FDA Devices Moderate Feb 17, 2021

Gown Isolation W/Ties Xl Blue, SKU 2201PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier pro…

FDA Devices Moderate Feb 17, 2021

Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K

FDA Devices Moderate Feb 17, 2021

Gown Isolation W/Ties Univ Blu, SKU 1200PG, 2200PG, 552200PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide …

FDA Devices Moderate Feb 17, 2021

ChemoPlus Drug Spill Kit-INSTI, SKU DP5016K

FDA Devices Moderate Feb 17, 2021

Lab Coats SMS 2X-Large White, SKU 2304LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier prot…

FDA Devices Moderate Feb 17, 2021

Covidien ChemoPlus Chemo Spill Kit, Nonsterile, SKU DP5108K

FDA Devices Moderate Feb 17, 2021

ChemoPlus" Chemo Prep & Admin Kit, CT4025

FDA Devices Moderate Feb 17, 2021

Gown Isolation W/Ties Xl Ylw, SKU 1101PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier prot…

FDA Devices Moderate Nov 25, 2020

Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutriti…

FDA Devices Moderate Nov 25, 2020

Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritio…

FDA Devices Moderate Nov 11, 2020

Covidien MONOJECT Standard Hypodermic Needle, Polypropylene Hub 22 G x 3/4". Intended use to facilitate activities such as: withdrawal of medication …

FDA Devices Moderate Oct 7, 2020

KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic …

FDA Devices Moderate Jul 15, 2020

Cardinal Health NPWT Canister with Gel 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, …

FDA Devices Moderate Mar 18, 2020

Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 - Product Usage: used for general purpose injection and aspiration of fluids from vial…

FDA Devices Moderate Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general purpose injection and aspirati…

FDA Devices Moderate Mar 18, 2020

Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and aspiration of fluids from via…

FDA Devices Moderate Feb 26, 2020

Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020. …

FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062

FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer Private Label Item Code: 3069

FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000

FDA Devices Moderate Feb 12, 2020

Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle Item code: 8881200029

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045

FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011

FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389

FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522

FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Cardinal Health 200, LLC 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