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 11 critical, 39 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 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 Aug 25, 2021 to Feb 14, 2024.

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 Critical Feb 14, 2024

Cardinal Health Monoject, 6ML Enteral Syringe (purple) Low Dose (LDT) - For Use with ENFit Connection System, REF 406SE

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 3 mL Syringe Luer-Lock Tip Soft Pack, REF 1180300777

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, REF 1180100777

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 12mL Enteral Syringe (purple) For Use with ENFit Connection System, REF 412SE

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 6 mL Syringe Luer-Lock Tip Soft Pack, REF 1180600777

FDA Devices Moderate Jan 24, 2024

CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510

FDA Devices Moderate Jan 24, 2024

Cardinal Health Suction Canister Liner, MEDI-VAC CRD 1000 mL Suction Canister Liner Kit with 6 mm 1.8 m Tube, REF 65651-517

FDA Devices Moderate Jan 24, 2024

Cardinal Health MEDI-VAC CRD Suction Canister Liner, 1000 mL Suction Canister Liner Kit with 5 mm 1.8 m Tube, REF 65651-516

FDA Devices Critical Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

FDA Devices Critical Nov 1, 2023

Monoject 20 mL Syringe Luer-Lock Tip Soft Pack

FDA Devices Critical Nov 1, 2023

Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack

FDA Devices Critical Nov 1, 2023

Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack

FDA Devices Critical Nov 1, 2023

Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack

FDA Devices Moderate Oct 25, 2023

Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

FDA Devices Moderate Oct 18, 2023

Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.

FDA Devices Moderate Oct 18, 2023

Procedure pack: Presource PBDS, Cat. PEMHEEESR, Southeast Hospital MHHS, Kit, ENT, SE, Sterile.

FDA Devices Moderate Oct 18, 2023

Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block Tray, Catalog SNE37ANMO…

FDA Devices Moderate Oct 18, 2023

Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip, Sterile; (3) Preso…

FDA Devices Moderate Oct 18, 2023

Procedure packs: (1) Presource PBDS, Cat. PGMHSUESR, Southeast Hospital MHHS, Kit, Set Up No Drape, SE, Sterile; (2) Presource PBDS Cat. PGVGLBP2…

FDA Devices Moderate Jun 14, 2023

Presource Kit, SMA21LPUHJ GYN Laparoscopy Pack. Convenience kit used for Laparoscopic surgery

FDA Devices Moderate Mar 1, 2023

Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A

FDA Devices Moderate Mar 1, 2023

Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2189

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2233

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2217

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2223

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2227

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2212

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2225

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2190

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2187

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2214

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2186

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2230

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 28 Fr, REF JP-2290

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2228

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2213

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 7 mm, REF JP-2211

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2191

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2232

FDA Devices Moderate Jan 25, 2023

Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2226

FDA Devices Moderate Nov 16, 2022

Cardinal Health GEL PACK REUSABLE, SMALL, Cat. 70204

FDA Devices Moderate Nov 16, 2022

Cardinal Health INSULATED GEL PACK REUSABLE, EXTRA LARGE, Cat. 80600

FDA Devices Moderate Nov 16, 2022

Cardinal Health Reusable Gel Pack, Hot/Cold Pack, 4.5 in. x 10 in., REF 70304A

FDA Devices Moderate Nov 16, 2022

Cardinal Health INSULATED GEL PACK REUSABLE, SMALL, Cat. 80204A

FDA Devices Moderate Nov 16, 2022

Cardinal Health INSULATED GEL PACK REUSABLE, MEDIUM, Cat. 80304A

FDA Devices Moderate Nov 16, 2022

Cardinal Health GEL PACK REUSABLE, EXTRA SMALL, Cat. 61115

FDA Devices Moderate Apr 20, 2022

Cardinal Health PROTEXIS PI and PI Classic, Surgical Gloves

FDA Devices Critical Aug 25, 2021

Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part number 73-1811). Intended for use to insert an Umbilical Venous Catheter (UVC) …

Nearby Manufacturers

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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