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Mckesson Medical-Surgical Inc. Corporate Office Recalls
276 recalls on record · July 28, 2021 to August 27, 2025 · Drugs, Medical Devices
Recalls by year
21
22
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25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 27, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020
Hazard: Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.
July 30, 2025DrugsFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Hazard: CGMP Deviations; potential temperature excursions due to transit delays
July 30, 2025DrugsFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc.,
Hazard: CGMP Deviations; potential temperature excursions due to transit delays
July 30, 2025DrugsFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks,
Hazard: CGMP Deviations; potential temperature excursions due to transit delays
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls HEMOCUE INC GLUC AQUEOUS 1HI/LO HEMCUE CONTROL KIT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ALINITY I ANTI-CCPS REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ALINITY I FREE PSA US(200TEST/EA) REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT FREE T4ABBDIA CALIBRATOR.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT TOTAL T36X4ML CALIBRATOR.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT VITAMIND 6LEVEL CALIBRATOR.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT HBSAG ASSAY(100TST/BX) BDS REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT POINT OF CARE TEST CREA I-STAT (25/BX) ABBTPT CARTRIDGE.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT HIV COMBO 1X4ML CALIBRATOR.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARC T-UPTAKE ASSAY (100TST/BX) ABBDIA REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARC ANTI-TPO ASSAY 100TST B REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS PROBE CONDITIONING F/ARCHITECT ANLYZ ABBDIA SOLUTION.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARC CARBON DIOXIDE6X5ML B CALIBRATOR.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls HEMOCUE INC HEMOTROL HIGH 2X1ML LEVEL 3 HEMCUE CONTROL.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls HEMOCUE INC HEMOTROL LOW 2X1ML LEVEL 1 HEMCUE CONTROL.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC ANTI-B BIOCLONE 10ML3X10ML.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC TOTAL BILI-ALKP XT (L-SEQUESTER) (300/PK) REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC FS(3PK/BX)ORCLNL DILUENT PACK 3.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC VANCOMYCIN (300/BX)ORCLNL REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS (60/CR 5CR/PK) ORCLNL REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ORTHO CLINICAL DIAGNOSTICS INC VITROS CALCIUM (L-SEQUESTER) (300/PK) REAGENT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT RAPID DX N AMERICA LLC HBA1C HEMOGLOBIN AFINION GLYCTD (15TST/BX) TEST KIT.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.