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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.

February 12, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063
Hazard: The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (¿ 0.2¿C for Genius 2 and ¿ 0.3¿C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2¿C for Genius 2 or +0.3¿C for Genius 3.
February 12, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062
Hazard: The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (¿ 0.2¿C for Genius 2 and ¿ 0.3¿C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2¿C for Genius 2 or +0.3¿C for Genius 3.
February 12, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013
Hazard: The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (¿ 0.2¿C for Genius 2 and ¿ 0.3¿C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2¿C for Genius 2 or +0.3¿C for Genius 3.
February 12, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
Hazard: The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (¿ 0.2¿C for Genius 2 and ¿ 0.3¿C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2¿C for Genius 2 or +0.3¿C for Genius 3.
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle Item code: 8881200029
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
July 31, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011
Hazard: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
May 15, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits a
Hazard: Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
May 15, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are
Hazard: Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
May 15, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-
Hazard: Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
May 15, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-u
Hazard: Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
March 6, 2019Medical DevicesFDA
Cardinal Health 200, LLC recalls Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for
Hazard: Curity All Purpose Sponges were not sterilized and distributed
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 9.0 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 8.5 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.
December 26, 2018Medical DevicesFDA
Cardinal Health 200, LLC recalls Protexis Neoprene Surgical Glove, Size 8.0 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 7.5 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.