Medical DeviceNov 1, 2023
Cardinal Health 200 Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack recall — FDA Z-0147-2024
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Class IFDA: OngoingCardinal Health 200, LLC
Recall history in this database
Classification mix: Class II: 208, Class I: 28.
Medical DeviceNov 1, 2023
Cardinal Health 200 Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack recall — FDA Z-0146-2024
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Class IFDA: OngoingCardinal Health 200, LLC
Medical DeviceNov 1, 2023
Cardinal Health 200 Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack recall — FDA Z-0149-2024
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Class IFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 25, 2023
Cardinal Health 200 Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model recall — FDA Z-0112-2024
Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure pack: Presource PBDS Cat recall — FDA Z-0090-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure pack: Presource PBDS, Cat recall — FDA Z-0085-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced recall — FDA Z-0083-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0091-2024
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Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS, Cat recall — FDA Z-0087-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Presource Fistulogram Pack, Cat recall — FDA Z-0092-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS, Cat recall — FDA Z-0084-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0089-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource Portacath Pack, Cat recall — FDA Z-0088-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0086-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceMar 1, 2023
Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG # recall — FDA Z-1158-2023
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…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceMar 1, 2023
Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E recall — FDA Z-1159-2023
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…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceMar 1, 2023
Cardinal Health Presource Packs IV START KIT- Intended for IV access device CATALOG # recall — FDA Z-1157-2023
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…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292 recall — FDA Z-0994-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2189 recall — FDA Z-0970-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2233 recall — FDA Z-0991-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2217 recall — FDA Z-0980-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2223 recall — FDA Z-0982-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2227 recall — FDA Z-0985-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 25, 2023
Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2212 recall — FDA Z-0975-2023
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains,…
Class IIFDA: OngoingCardinal Health 200, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Cardinal Health 200, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.