PlainRecalls

Mckesson Medical-Surgical Inc. Corporate Office

276 recalls on record · Latest: Aug 27, 2025

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Agency notice ledger

Federal filing book Mckesson Medical-Surgical I… HEAVY-BOOK · MULTI-AGENCY

#41 of 14,151 · 276 notices · 0.264% archive

  • BOOK 276 notices
  • RANK #41 of 14,151
  • SHARE 0.264% archive
  • AGENCY FDA Drug (157)
  • CAT drugs
  • CATS 4 categories
  • LATEST Aug 27, 2025
  • PHOTO Toyota

Nearest notice-volume peer: Toyota (5 notice gap)

Mckesson Medical-Surgical Inc. Corporate Office accounts for about 0.264% of the 104,423-notice archive on 276 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Mckesson Medical-Surgical I… sits among 14,151 recalling firms

Mckesson Medical-Surgical Inc. Corporate Office ranks 41st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Mckesson Medical-Surgical I… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

276 41st of 14151 higher than 14,110 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Mckesson Medical-Surgical I… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Mckesson Medical-Surgical Inc. Corporate Office holds about 0.264% of archive notices alongside 276 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 276 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

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 55513-880-02.

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., Princeton, NJ 08540, Distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product of Canada, NDC 54643-5649-1

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 08520, NDC 55150-0330-01

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., 12390 El Camino Real San Diego California 92130, Distributed by Antares Pharma, Inc., Ewing, NJ NDC 18657-117-04

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 strips, microalbumin, and creatinine by listed test methods.

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 Number: 8881560125

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 mL

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

Mckesson Medical-Surgical I… carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (276 here — heavy-book).

Similar drugs volume

Nearest multi-notice firms sharing this firm's wide category mix.

Frequently Asked Questions

How many federal recall notices name Mckesson Medical-Surgical I…?
PlainRecalls indexes 276 distinct federal recall events naming Mckesson Medical-Surgical Inc. Corporate Office, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Mckesson Medical-Surgical I… sit among other recalling firms?
Mckesson Medical-Surgical Inc. Corporate Office ranks #41 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Mckesson Medical-Surgical I…'s notices?
FDA Drug accounts for 157 of this firm's 276 indexed notices across 2 issuing agencies.
What product category dominates Mckesson Medical-Surgical I…'s filing book?
Filings for Mckesson Medical-Surgical Inc. Corporate Office span 4 product categories, led by drugs. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Mckesson Medical-Surgical Inc. Corporate Office: 276 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Drug). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Mckesson Medical-Surgical Inc. Corporate Office; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026