PlainRecalls

Mckesson Medical-Surgical Inc. Corporate Office

Compiled from official public sources by the editorial team.

276 recalls on record · Latest: Aug 27, 2025

Mckesson Medical-Surgical Inc. Corporate Office Recall Insight

Mckesson Medical-Surgical Inc. Corporate Office appears on 276 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.271% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Aug 27, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 2 distinct product categories, with issuing agencies dominated by FDA Devices (40), FDA Drug (10). The date window on this page runs from Mar 20, 2024 to Aug 27, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Aug 27, 2025

Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020

FDA Drug Moderate Jul 30, 2025

EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC …

FDA Drug Moderate Jul 30, 2025

BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.

FDA Drug Moderate Jul 30, 2025

PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21

FDA Devices Moderate Jun 4, 2025

SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.

FDA Devices Moderate Jun 4, 2025

ABBOTT POINT OF CARE TEST CREA I-STAT (25/BX) ABBTPT CARTRIDGE.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC ANTI-B BIOCLONE 10ML3X10ML.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT FREE T4ABBDIA CALIBRATOR.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC ANTI-TPO ASSAY 100TST B REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC, TEST CHOLESTEC LDXLIPID PROFILE (10/BX 50BX/CS) CASSETTES.

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC GLUC AQUEOUS 1HI/LO HEMCUE CONTROL KIT.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS CALCIUM (L-SEQUESTER) (300/PK) REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC CARBON DIOXIDE6X5ML B CALIBRATOR.

FDA Devices Moderate Jun 4, 2025

BD MICROBIOLOGY FLUID THIOGLYCOLLATE MED TUBE 1004321196 (100/CT) MEDIA.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT HBSAG ASSAY(100TST/BX) BDS REAGENT.

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL LOW 2X1ML LEVEL 1 HEMCUE CONTROL.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC T-UPTAKE ASSAY (100TST/BX) ABBDIA REAGENT.

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT VITAMIND 6LEVEL CALIBRATOR.

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL HIGH 2X1ML LEVEL 3 HEMCUE CONTROL.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS (60/CR 5CR/PK) ORCLNL REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ALINITY I FREE PSA US(200TEST/EA) REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS PROBE CONDITIONING F/ARCHITECT ANLYZ ABBDIA SOLUTION.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT TOTAL T36X4ML CALIBRATOR.

FDA Devices Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC CHOLESTECH LDX LIPID PROFILE+GLUCOSE (10/BX 50BX/CS) TEST.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT HIV COMBO 1X4ML CALIBRATOR.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VANCOMYCIN (300/BX)ORCLNL REAGENT.

FDA Devices Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC HBA1C HEMOGLOBIN AFINION GLYCTD (15TST/BX) TEST KIT.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC FS(3PK/BX)ORCLNL DILUENT PACK 3.

FDA Devices Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC MULTI ANALYTE LVL1&2250UL CHOLS CONTROL

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC TOTAL BILI-ALKP XT (L-SEQUESTER) (300/PK) REAGENT.

FDA Devices Moderate Jun 4, 2025

BD MICROBIOLOGY MAC CONKEY II AGAR (100/CT) 21270 MEDIA.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ALINITY I ANTI-CCPS REAGENT.

FDA Drug Moderate May 7, 2025

Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, Manufactured for: Sandoz Inc.,…

FDA Drug Moderate May 7, 2025

Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ …

FDA Drug Moderate Dec 18, 2024

Hylenex recombinant (hyaluronidase) injection, 150 USP units/mL, 4x1 mL Single Dose Vials, Rx only, Manufactured for and marketed by Halozyme, Inc., …

FDA Devices Moderate Oct 30, 2024

Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing Levels 1 & 2 6 X 15 mL-IVD intended as a control for urinalysis reagent …

FDA Drug Moderate Oct 2, 2024

Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06

FDA Devices Moderate Jun 19, 2024

Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog…

FDA Devices Moderate Mar 27, 2024

Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

FDA Devices Moderate Mar 27, 2024

Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis

FDA Devices Moderate Mar 27, 2024

Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL

FDA Devices Moderate Mar 27, 2024

Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 …

FDA Devices Moderate Mar 27, 2024

Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL

FDA Drug Moderate Mar 20, 2024

Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC 60793-0701-10

FDA Drug Moderate Mar 20, 2024

Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10

FDA Drug Moderate Mar 20, 2024

Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.