Manufacturer
275 recalls in our database name Mckesson Medical-Surgical Inc. Corporate Office as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Due to an inventory system error, Clearview Strep A Exact II diagnostic kits were shipped to facilities without the required license to purchase them.
Mckesson is recalling EVENITY (romosozumab-aqqg) injectable medication due to manufacturing compliance deviations and potential temperature excursions during shipping. The recall affects lot 1178382 distributed to Ohio, Virginia, and Florida.
McKesson Medical-Surgical is recalling BENLYSTA (belimumab) due to potential temperature excursions during transit that may affect drug potency. The recall involves product distributed in Ohio, Virginia, and Florida.
Mckesson is recalling PROLIA (denosumab) 60mg/mL pre-filled syringes (lot 1180924) due to CGMP manufacturing deviations and potential temperature excursions during transit in Ohio, Virginia, and Florida.
Abbott diagnostic calibrators may have been stored improperly during transit delays caused by thunderstorms, potentially affecting test accuracy. The units are being recalled to prevent inaccurate or delayed diagnostic test results.
Ortho Clinical Diagnostics' VITROS Calcium reagent (300-pack) is being recalled due to transit delays from severe thunderstorms that may have exposed the product to temperatures outside recommended storage conditions, potentially affecting test accuracy.
Ortho Clinical Diagnostics diluent packs may have been stored outside recommended cold-chain conditions during transit due to severe thunderstorms. This could lead to incorrect or delayed test results.
Abbott probe conditioning solution recalled after cold chain failure during transit. Products exposed to improper storage temperatures may produce inaccurate or delayed test results.
Abbott Diagnostics is recalling Alinity I Anti-CCPS Reagent after shipments may have been stored outside recommended temperature conditions during transit. This could result in incorrect or delayed test results.
Abbott Diagnostics VitaminD Calibrator units may have been exposed to improper storage temperatures during transit delays caused by severe thunderstorms. This could result in inaccurate or delayed test results.
Abbott HbA1c test kits were stored outside recommended cold chain conditions during transit delays caused by severe thunderstorms, risking incorrect or delayed test results. Eight units were affected.
Mckesson is recalling Cholestech LDX Lipid Profile and Glucose test kits due to transit delays from severe thunderstorms that may have caused improper storage. The recall addresses the risk of incorrect or delayed test results.
Cold chain storage failures during transit of Abbott Diagnostics Alinity I Free PSA reagent, caused by severe thunderstorms, may result in incorrect or delayed test results. Units were distributed across 11 U.S. states.
Ortho Clinical Diagnostics VITROS BUN reagent distributed nationwide may have been stored outside recommended conditions during transit due to severe thunderstorms, potentially causing incorrect or delayed test results.
A Sekisui Diagnostics HCG control set used in clinical laboratories may have been exposed to improper storage temperatures during transit due to severe thunderstorms. This exposure could result in incorrect or delayed test results.
Cold chain failures during transit may have compromised HemoCue glucose analyzer microcuvettes, potentially causing incorrect or delayed test results. Affected units were distributed nationwide to healthcare facilities.
McKesson Medical-Surgical is recalling Abbott Cholestec LDX Lipid Profile test cassettes that were exposed to temperatures outside recommended storage conditions during transit delays. This could result in incorrect or delayed test results.
Abbott Diagnostics Anti-TPO assay reagent was recalled after transit delays caused storage outside recommended cold chain conditions, potentially resulting in incorrect or delayed test results.
HEMOCUE Hemotrol High quality control material is being recalled due to transit delays caused by severe thunderstorms that may have resulted in improper storage conditions, potentially affecting test accuracy.
A laboratory reagent was recalled because weather-related transit delays caused it to be stored outside recommended temperature conditions. This could result in incorrect or delayed diagnostic test results.
Mckesson is recalling ORTHO CLINICAL DIAGNOSTICS vancomycin reagent due to transit delays caused by severe thunderstorms that may have exposed products to improper storage conditions, potentially resulting in inaccurate or delayed test results.
Abbott diagnostics calibrators were exposed to improper storage temperatures during transit due to severe thunderstorms, which may cause incorrect or delayed HIV test results.
Abbott Diagnostics ARCH AUSAB ANTI-HBS reagent is being recalled due to cold chain storage failures caused by transit delays. Exposure to temperatures outside labeled requirements may increase the risk of incorrect or delayed test results.
Abbott Diagnostics Architect Progesterone reagent units were affected by transit delays during severe thunderstorms, causing improper storage that could lead to incorrect or delayed test results.
Abbott Rapid DX diagnostic control products were improperly stored during transit due to severe thunderstorms, which may cause inaccurate or delayed test results.