Mckesson Medical-Surgical Inc. Corporate Office recalls
Every recall we track for Mckesson Medical-Surgical Inc. Corporate Office — 276 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Mckesson Medical-Surgical Inc. Corporate Office more than tripled in 2025 (38, up from 12 in 2024).
All FDA recall records for Mckesson Medical-Surgical Inc. Corporate Office since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 6 | 140 | 79 | 225 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 9 | 3 | 12 |
| 2025 | 0 | 1 | 37 | 0 | 38 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Mckesson Medical-Surgical Inc. Corporate Office recalls
What to do if you have a recalled Mckesson Medical-Surgical Inc. Corporate Office product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Mckesson Medical-Surgical Inc. Corporate Office recalls
15 shown- Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020
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 Medical-SurgicalJul 30, 2025 - Use cautionDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile,
Baxter recalls specific lots of Infuvite Adult injection due to potential cold chain breaches during transit. Check lot numbers AA2279 and AA2383.
BaxterApr 25, 2025 - Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.
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.
SEKISUI DIAGNOSTICSApr 24, 2025 - Lower riskDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc.,
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-SurgicalApr 21, 2025 - Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing Levels 1 & 2 6 X 15 mL-IVD intended as a
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.
Mckesson Medical-SurgicalSep 17, 2024 - UnratedDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC
Mckesson recalls 15mL Proparacaine Hydrochloride Ophthalmic Solution (0.5%) due to temperature abuse risk. Products exposed to improper temperatures above label specs may be unsafe.
Mckesson Medical-SurgicalSep 11, 2024 - UnratedDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Hylenex recombinant (hyaluronidase) injection, 150 USP units/mL, 4x1 mL Single Dose Vials, Rx only, Manufactured for
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.
HalozymeSep 11, 2024 - UnratedMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog
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 Medical-SurgicalApr 23, 2024 - Lower riskDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer
Mckesson recalls Pfizer's Bicillin L-A injections due to improper storage conditions. Affected products may have label deviations. Consumers should check NDC numbers and contact pharmacy for details.
Mckesson Medical-SurgicalFeb 7, 2024 - Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
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.
SterisJan 9, 2024 - UnratedDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye drops, Eye Itch Relief, up to 12
Mckesson Medical-Surgical recalls Systane Zaditor eye drops (0.035% ketotifen fumarate) because they were stored outside label specifications. This may affect product safety.
Mckesson Medical-SurgicalJun 29, 2022 - Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll Ethylene Oxide (EO) Gas / Steam 3 Inch X 100
Mckesson Medical-Surgical recalls Sani-Roll sterilization rolls produced between June 1 and September 30, 2021, due to potential temperature excursions affecting product effectiveness.
Mckesson Medical-SurgicalMay 25, 2022 - Lower riskMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50
Mckesson Medical-Surgical recalls Coag-Sense PT/INR test kits produced between May 30 and August 24, 2021, due to potential temperature excursions affecting product effectiveness. Consumers should check lot codes and contact for guidance.
Mckesson Medical-SurgicalMay 25, 2022 - Use cautionDrug
Mckesson Medical-Surgical Inc. Corporate Office recalls Thrombin JMI, Vial 5,000IU 2/diluent, kit, Rx only, MFG: Pfizer NDC 60793-215-05
McKesson recalls 157 Thrombin JMI vial kits due to cGMP temperature abuse deviations. Check your prescription details.
Thrombin JMIApr 13, 2022 - UnratedMedical device
Mckesson Medical-Surgical Inc. Corporate Office recalls ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine
Mckesson Medical-Surgical recalls Moderna 140-dose vaccine convenience kits with unsuitable 3mL syringes that could cause injury during vaccine administration.
Mckesson Medical-SurgicalJun 2, 2021
Mckesson Medical-Surgical Inc. Corporate Office recall questions
How many recalls has Mckesson Medical-Surgical Inc. Corporate Office had?
276 recalls from Mckesson Medical-Surgical Inc. Corporate Office are on record with U.S. safety agencies, from 2021–2025 (157 drug, 119 medical device).
What is the most recent Mckesson Medical-Surgical Inc. Corporate Office recall?
Mckesson Medical-Surgical Inc. Corporate Office recalls Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020, dated Jul 30, 2025. Every Mckesson Medical-Surgical Inc. Corporate Office recall is listed on this page, newest first.
Why are Mckesson Medical-Surgical Inc. Corporate Office products recalled?
The most common reasons on record: cGMP deviations: Temperature abuse (130); CGMP Deviations: products were stored outside the drug label specifications. (17); CGMP Deviations; potential temperature excursions due to transit delays (3); cGMP Deviations: Products were stored outside the drug label specifications. (3).
What should I do if I have a recalled Mckesson Medical-Surgical Inc. Corporate Office product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Mckesson Medical-Surgical Inc. Corporate Office recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.