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Cardinal Health 200 Recalls
285 recalls on record · October 19, 2016 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 20 mL Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
November 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
Hazard: Demonstrated recognition and compatibility issues with syringe infusion pumps.
October 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Hazard: Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource Fistulogram Pack, Cat. SANOCFGHHA, Hartford Hospital, Sterile.
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Ant
Hazard: XXX
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PNVMNIB21, Kit, Neuro IMAS, Sterile; (2) Presource PBDS Cat. PN08LAG13, Kit
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource Portacath Pack, Cat. SANV1PIFSB, Medstar Franklin Square Med CE, Sterile; and (2) Pre
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS, Cat. PGMHSUESR, Southeast Hospital MHHS, Kit, Set Up No Drape, SE, Sterile; (2)
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PG33BTO21, Ohio State Univ Wexner Med Ctr, Kit, Roux UH, Sterile; (2) Pres
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure pack: Presource PBDS, Cat. PEMHEEESR, Southeast Hospital MHHS, Kit, ENT, SE, Sterile.
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS, Cat. PC71EXOU7, Ohio State Univ Wexner Med Ctr, Kit, Extraction Ross, Sterile;
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
October 18, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource
Hazard: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
July 26, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls NovaPlus Infant Heel Warmer, Instant Squeeze Activation, Catalog Number V11460-010
Hazard: Cardinal Health has received an increase in burst/leaking complaints from mid-April to May regarding the above listed lot of the Novalplus Infant Heel Warmer with tape.
June 14, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource Kit, SMA21LPUHJ GYN Laparoscopy Pack. Convenience kit used for Laparoscopic surgery
Hazard: Inadvertently released for distibution without sterility assurance.
March 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E
Hazard: Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
March 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A
Hazard: Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
March 1, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Packs IV START KIT- Intended for IV access device CATALOG #: 01-5798B
Hazard: Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 28 Fr, REF JP-2290
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 24 Fr, REF JP-2234
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2233
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2232
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2231
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2230
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.
January 25, 2023Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2229
Hazard: Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.