Every recall we track for Mckesson Medical-Surgical Inc. Corporate Office — 276 in all — plus the complaints and injury reports the public filed about them.
Mckesson Medical-Surgical recalls Clearview Strep A Exact II Dipstick Respiratory Kit (Catalog 4581225020) due to shipping devices without proper license classification. All units are affected.
Mckesson recalls 150 mg/mL Medroxyprogesterone Acetate injectable vials shipped from India in April 2025 due to storage delays. Products may have been improperly stored, risking safety and quality. Check NDC 55150-0330-01 and lot 1MP24042.
Baxter recalls Infuvite Adult multiple vitamins injections that may have been improperly stored during transit due to thunderstorms, risking product safety and effectiveness.
Abbott Diagnostics recalls Alinity I Anti-CCPS reagent due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Learn if your product is affected.
BD Microbiology MacConkey II Agar (21270) may cause incorrect or delayed test results if stored outside recommended conditions due to transit delays from severe thunderstorms. Affected units were sold with specific catalog and GTIN numbers.
Ortho Clinical Diagnostics recalls Total Bili-Alkp Xt reagent due to potential test errors from improper cold storage during transit. Affected units may have incorrect or delayed results.
Abbott's Multi-Analyte Lvl1&2250UL Cholesterol Control devices may give incorrect results if stored outside recommended conditions due to recent severe thunderstorms. Affected units were sold with specific catalog and GTIN numbers.
Ortho Clinical Diagnostics recalls Diluent Pack 3 due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Consumers should check product details and contact the manufacturer.
Abbott HbA1c test kits recalled due to transit delays causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected kits.
Ortho Clinical Diagnostics recalls Vancomycin reagent due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details to see if affected.
Abbott Diagnostics recalls HIV Combo : transit delays during thunderstorms may cause improper storage, risking incorrect or delayed HIV test results. Affected units include specific catalog and GTIN numbers.
Abbott recalls Cholestech LDX lipid profile and glucose test kits that may produce incorrect results due to storage issues from transit delays during severe thunderstorms. Consumers should check product labels for catalog number 97991 or GTIN 893038002937.
Abbott Diagnostics recalls Architect Total T36X4ML calibrators due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Affected units have specific catalog and GTIN numbers.
Abbott Diagnostics probe conditioning solution may have been stored outside recommended conditions due to thunderstorms, risking incorrect or delayed test results. Affected units include specific catalog and GTIN numbers.
Abbott Diagnostics recalls Alinity I Free PSA reagents due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Consumers should check product details and contact Abbott for guidance.
Ortho Clinical Diagnostics recalls Vitros Phosphorus reagents due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Affected units have specific catalog and order numbers.
Mckesson Medical-Surgical recalls HEMOCUE HEMOTROL High 2x1ml Level 3 due to potential cold chain disruptions from severe thunderstorms, which could lead to incorrect or delayed test results. Affected units were sold with specific catalog and GTIN numbers.
Recall of Abbott Architect Vitamin D 6-Level Calibrator due to transit delays causing improper storage. May lead to incorrect or delayed test results. Check product details for affected units.
HEMOCUE Glucose Analyzer Microcuvette units may give incorrect or delayed results if stored outside recommended conditions due to transit delays from thunderstorms. Affected units have specific catalog and order numbers.
Abbott recalls ARC T-Uptake Assay reagents due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected units.
HEMOCUE HEMOTROL Low 2x1ml Level 1 Control units may have been stored outside recommended cold conditions due to storm delays, potentially causing incorrect or delayed test results. Affected units were sold with specific catalog and GTIN numbers.
Abbott Diagnostics recalls Architect HBSAG Assay reagents due to transit delays during thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Affected units include specific catalog and GTIN numbers.
BD Microbiology Fluid Thio glycolate media tubes may cause incorrect or delayed test results due to storage issues from thunderstorms. Affected units include specific model numbers sold through certain channels.
Abbott Diagnostics recalls ARC Carbon Dioxide 6x5ml B Calibrator due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected units.
Ortho Clinical Diagnostics recalls Vitros Calcium (L-Sequester) reagents due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Consumers should check product details and contact the manufacturer for guidance.
HEMOCUE Glucose Test Kits may give incorrect results if stored outside recommended conditions due to transit delays from thunderstorms. Affected kits include specific model numbers and order details.
Abbott recalls lipid profile test cassettes that may cause incorrect or delayed results due to storage issues from severe thunderstorms. Consumers should check product details and contact Abbott for guidance.
Abbott Diagnostics recalls ARC Anti-TPO Assay 100TST B reagent due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected units.
Abbott Diagnostics recalls Architect Free T4ABBDIA Calibrator due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Affected units have specific catalog and GTIN numbers.
Abbott Diagnostics recalls 100-test progestrone reagent due to transit delays causing improper storage. This may lead to incorrect or delayed test results. Affected units have specific catalog and order numbers.
Recall of Abbott Diagnostics Arch Ausab Anti-HBs reagent due to transit delays causing improper storage. May lead to incorrect or delayed test results.
Ortho Clinical Diagnostics recalls Vitros BUN reagents due to transit delays during thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected items.
Ortho Clinical Diagnostics recalls Bioclone 1:10ml test kits due to potential storage issues from thunderstorms. Products may give incorrect or delayed test results if not kept at proper cold temperatures.
Abbott recalls specific I-STAT Crea test cartridges that may cause incorrect or delayed test results if stored outside recommended conditions due to transit delays from severe thunderstorms.
SEKIS: HCG control set recall due to cold chain disruptions from thunderstorms. Products may give incorrect or delayed test results if stored outside recommended conditions. Check catalog number 138 for affected items.
Mckesson Medical-Surgical recalls PROLIA (denosumab) injections due to possible temperature excursions during shipping. Affected lots may have been exposed to unsafe temperatures.
Mckesson recalls BENLYSTA 400 mg/20 mL vials (NDC 49401-102-01) due to potential temperature excursions during transit. This may affect drug stability.
Mckesson Medical-Surgical recalls EVENITY (romosozumab) injections due to possible temperature excursions during shipping. Affected lots may have been exposed to temperatures outside safe ranges, risking product stability.
Mckesson Medical-Surgical recalls Quantimetrix Urine Chemistry Control Sets due to potential temperature exposure causing delayed patient test results. Affected units may have been shipped without proper packaging.
Hylenex recombinant hyaluronidase injection vials recalled due to temperature excursions during manufacturing. Affected vials have specific NDC and serial numbers. Consumers should contact the manufacturer for details.
Mckesson Medical-Surgical recalls Coviden Monoject 60ml syringes due to inadvertent distribution of quarantined product. Affected units have specific catalog numbers and lot codes.
Mckesson recalls Infuvite Adult Multiple vitamins injection vials due to improper storage conditions. Affected products were stored outside label specifications. No remedy provided in official notice.
Abbott recalls i-STAT Level 3 1.7mL test kits that may have experienced temperature excursions in walk-in refrigerators, potentially causing incorrect or delayed test results. Affected units were sold from January 2024.
Abbott's Reproductive Endocrinology Control Set may give incorrect pregnancy test results if stored in a refrigerator that gets too cold. Recalled due to temperature excursions on Jan 8, 2:00 PM.
Abbott recalls i-STAT Level 1 test kits that may have been stored in refrigerators with temperature issues, potentially causing incorrect or delayed test results. Affected kits were sold in specific lots and may require replacement.
Recalled Sekisui Diagnostics BVBLUE Bacterial Vaginosis test kits may have been stored at unsafe temperatures, risking inaccurate results. Consumers should check kit details and contact manufacturer for guidance.
Steris Corporation recalls Endo Cleaning Indicator VERIFY" RESITEST" due to temperature excursions in refrigerators causing potential incorrect or delayed test results. Affected units sold in the U.S. from January 2024.
A&D Original Ointment, Diaper Rash O:16 oz jars recalled due to improper storage conditions. Consumers should check labels for NDC 11523-0096-3.
Alcon recalls Systane Balance lubricant eye drops due to improper storage conditions. Products may not meet drug label specifications.
Mckesson recalls Systane lubricant eye drops due to improper storage conditions. Products may not meet drug label specifications. Consumers should check NDC codes and contact Mckesson for details.
Health Star Bisacodyl suppositories (100 per box) recalled due to improper storage conditions. Consumers should check product labels for NDC 57896-443-01.
Mckesson Medical-Surgical recalls Naphcon A eye drops and antihistamine eye drops because they were stored outside drug label specifications. Consumers should check product labels for NDC 0065-0085-15.
Mckesson Medical-Surgical recalls Triple Antibiotic Ointment due to improper storage conditions. Products may not meet drug label specifications, potentially affecting safety.
Alcon's sterile eye wash solution (4 fl oz) was recalled due to improper storage conditions. Products stored outside label specifications may be contaminated. Consumers should check NDC 0065-0530-04 for affected items.
Mckesson recalls alcohol swabsticks due to storage outside drug label specifications. Products may not meet safety standards. Check NDC 67777-300-01 for affected items.
