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.
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 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.
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.
Abbott probe conditioning solution recalled after cold chain failure during transit. Products exposed to improper storage temperatures may produce inaccurate or delayed test results.
Mckesson Medical-Surgical is recalling BD Microbiology Fluid Thioglycollate Medium tubes due to transit delays and storage outside recommended temperature conditions. The products may produce incorrect or delayed test results.
HemoCue glucose control kits may have been exposed to improper storage temperatures during transit due to severe thunderstorms, which could result in inaccurate test results. Affected units were distributed nationwide in 10 states.
Mckesson Medical-Surgical Inc. is recalling VITROS phosphorus reagent due to improper storage during transit caused by severe thunderstorms. The storage deviation could affect test result accuracy.
Abbott Diagnostics ARC Carbon Dioxide 6x5mL calibrators distributed to ten US states may have been exposed to temperatures outside recommended storage conditions during transit, potentially affecting diagnostic test result accuracy.
This diagnostic calibrator may have been exposed to improper storage temperatures during transit due to severe thunderstorms, potentially affecting test result accuracy. Affected units were distributed to healthcare facilities across ten states.
Abbott Diagnostics ARC T-Uptake Assay units may have been stored outside recommended temperature conditions during transit delays caused by severe thunderstorms. Storage deviation could result in incorrect or delayed test results.
BD Microbiology MAC Conkey II Agar culture media was exposed to improper storage conditions during transit due to severe thunderstorms. This may cause inaccurate or delayed test results.
McKesson's Medroxyprogesterone Acetate Injectable Suspension is recalled due to cold chain failures from thunderstorms that may have compromised potency. The recall affects units distributed to medical facilities in Mississippi and Florida.
Infuvite Adult injectable vitamins distributed to medical facilities in Mississippi and Florida are being recalled due to shipping delays during severe thunderstorms that may have compromised storage conditions and product potency.
Mckesson Medical-Surgical Inc. is recalling HYLENEX RECOMBINANT (hyaluronidase) injection due to cGMP deviations involving a temperature excursion during storage, which may have compromised drug potency.
McKesson Medical-Surgical is recalling 27 bottles of Proparacaine Hydrochloride ophthalmic solution (lots 476261, 479751, 479741) due to temperature abuse that may have compromised sterility. Product was distributed to medical facilities in Maryland and Virginia.
Coviden Monoject 60ml Luer-Lock syringes were inadvertently distributed despite being quarantined. Mckesson Medical-Surgical is recalling approximately 100 units (lot 330737X) distributed in the United States.
Abbott's i-STAT Level 1 control device is recalled because a refrigerator temperature excursion on January 8, 2024, could cause incorrect or delayed test results. The walk-in storage unit failed, causing temperatures to fall below the required range of 35.6-46.4°F.
McKesson recalls Abbott Rapid Dx pregnancy test control sets due to a refrigerator temperature excursion that could cause inaccurate or delayed test results.
Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.
Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.
A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.
Mckesson is recalling Bicillin L-A prefilled syringes stored outside label specifications. The FDA Class II recall affects 70 vials distributed to direct accounts in NM, AZ, and UT.
Baxter Healthcare's Infuvite Adult Multiple Vitamins Injection is being recalled because 70 vials were stored outside their labeled specifications, potentially affecting product stability. The affected vials were distributed to three direct accounts in Arizona, New Mexico, and Utah.
McKesson Medical-Surgical is recalling Rocuronium Bromide Injection vials due to storage outside label specifications. Seventy vials were distributed to three healthcare accounts in New Mexico, Arizona, and Utah.
SPS Medical Supply Crosstex sterilization rolls (model SCT3) are being recalled because they were exposed to high temperatures during manufacturing facility storage before shipment. Temperature exposure may have compromised the product's sterilization effectiveness.