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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.
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 7.0 This powder-free sterile light brown colored surgeons gloves are a disposa
Hazard: Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 6.5 This powder-free Surgeon s glovessterile light brown colored surgeons glov
Hazard: Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 6.0 This powder-free sterile light brown colored surgeons gloves are a dispo
Hazard: Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a disposa
Hazard: Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, No Probe, Double Spike, Ref ASU1221, packaged 1/box, 12 boxes/case, single use,
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, No Probe, Single Spike, Ref ASU1220, packaged 1/box, 12 boxes/case, single use,
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Double Spike, Ref ASU1211, packaged 1/box, 12 boxes/case, sing
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, sing
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, packaged 1/box, 12 boxes/case, sing
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, sing
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Double Spike and no Probe, Ref ASC1221, packaged 1/
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Single Spike and no Probe, Ref ASC1220, packaged 1/
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Double Spike,
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Single Spike,
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve with Pulse Wave Cassette, Cassette Trumpet Valve with Bariatric Probe, Double Spike, Ref ABP1201
Hazard: The suction valve may not close properly which could cause continuous suction.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin pr
Hazard: A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource PBDS, Kit, No Spiro. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG
Hazard: A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG,
Hazard: A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
July 25, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep
Hazard: A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
May 9, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Medi-Vac(TM) Flex Advantage(TM) Suction Canister Liner, Material Numbers: a) REF 6561-910C b) REF 6561-916K c) REF 65
Hazard: products may be missing a one-way valve on the fluid patient port.
September 13, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific d
Hazard: The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.
August 30, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case
Hazard: Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
August 2, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical dr
Hazard: Outer label of some units of product number/lot number 8482, Lot 16LFS235 and product number/lot number 9414, Lot 16LUS317 do not match the drape packaged inside.
August 2, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan,
Hazard: Outer label of some units of product number/lot number 8482, Lot 16LFS235 and product number/lot number 9414, Lot 16LUS317 do not match the drape packaged inside.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Flat Drain, 10mm Full W/Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Dra
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Flat Drain, 7mm Full W/Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drai
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Round Drain, 19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Round Drain, 15FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Round Drain, 10FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
May 31, 2017Medical DevicesFDA
Cardinal Health 200, LLC recalls Jackson-Pratt Silicone Round Drain, 7FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems
Hazard: Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.