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Mckesson Medical-Surgical Inc. Corporate Office

Mckesson Medical-Surgical Inc. Corporate Office Recalls

All product recalls associated with Mckesson Medical-Surgical Inc. Corporate Office.

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Recall Summary

Total Recalls

268

Past Year

Class I (Serious)

Most Recent

Jul 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 241–260 of 268 recalls

Aparaclonidine Ophthalmic Solution 0.5% (Mckesson) – Temperature Deviation (2022)

cGMP deviations: Temperature abuse

Class IIModerate

FDAApr 13, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233: ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, ...

Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.

FDAJun 2, 2021Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Levetiracetam Tablets (McKesson) - Barcode Error (2021)

Labeling; Wrong Barcode; error in the machine-readable barcode which could result in some units being read as Naproxen Tablets 500 mg. Product is labeled correctly as Levetiracetam

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Class IIILow

FDAMay 26, 2021Nationwide• McKesson Corporation dba McKesson Drug Company

Docusate Sodium Softgels (McKesson) – label mix-up (2019)

Labeling: Label mix-up: Secondary carton may be labeled as Gabapentin 300mg instead of Docusate Sodium 100mg softgel caps.

Class IIModerate

FDAJan 16, 2019Nationwide• Rx Pak Division of McKesson Corporation

Megestrol Acetate Suspension (Mckesson) – Subpotent Drug (2018)

Supterpotent Drug

Class IIModerate

FDAAug 14, 2018Nationwide• Mckesson Corporation

Diltiazem HCl Capsules (McKesson) – Dissolution Failure (2018)

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Class IIILow

FDAApr 23, 2018Nationwide• Mckesson Packaging Services

Diltiazem CD Capsules (McKesson) – Dissolution Failure (2018)

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Class IIILow

FDAApr 23, 2018Nationwide• Mckesson Packaging Services

Diltiazem HCl Capsules (McKesson) – Dissolution Failure (2018)

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Class IIILow

FDAApr 23, 2018Nationwide• Mckesson Packaging Services

Ranitidine Tablets (Mckesson) – Stability Failure (2018)

Failed Stability Specifications

Class IIModerate

FDAFeb 26, 2018Nationwide• Mckesson Packaging Services

Megestrol Suspension (Mckesson) – Subpotent Drug (2018)

Subpotent Drug: Out of specification for assay (stability testing)

Class IIILow

FDAJan 29, 2018Nationwide• Mckesson Packaging Services

Propafenone Hydrochloride Tablets (Mckesson) – Moisture Limit Failure (2017)

Failed moisture limits: Out of specification for moisture content.

Class IIILow

FDAAug 28, 2017CO, IL, LA +2 more• Mckesson Packaging Services

BuPROPion HCL Tablets (Mckesson) – Moisture Limits (2017)

Failed Moisture Limits: Product tested out-of-specification for moisture content.

Class IIILow

FDAMay 30, 2017Nationwide• Mckesson Packaging Services

Hydralazine Injection (Mckesson) – Temperature Abuse (2017)

Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.

Class IIModerate

FDAMar 8, 2017Nationwide• Mckesson Medical Surgical

Aspirin Chewable Tablets (Mckesson) - Foreign Material Risk (2017)

Presence of Foreign Substance: foreign material found in the bulk inventory.

Class IIModerate

FDAFeb 23, 2017Nationwide• Mckesson Packaging Services

Donepezil HCl Tablets (Mckesson) – Subpotent (2017)

Supotent: Out of Specification result for assay test during routine stability testing.

Class IIILow

FDAJan 4, 2017CO, LA, OH• Mckesson Packaging Services

Xanax 0.5mg Tablets (Mckesson) – Missing Label (2016)

Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).

Class IIILow

FDASep 15, 2016CO, IL, LA +1 more• Mckesson Packaging Services

Lansoprazole Capsules (Mckesson) – Label Mix-up (2016)

Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.

Class IIILow

FDASep 8, 2016Nationwide• Mckesson Packaging Services

SKY Aspirin Chewables (Mckesson) – Labeling Mix-up (2016)

Labeling: Label mix-up -outer carton incorrectly labeled as aspirin chewable tablets.

Class IIILow

FDAApr 12, 2016Nationwide• Mckesson Packaging Services

McKesson Israel Ltd.: McKesson Cardiology ECG Management It is a software ap...

An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.

Class IIModerate

FDADec 19, 2014MA, MS, NH +3 more• McKesson Israel Ltd.

Amiodarone HCl Injection (Mckesson) – Temperature Storage Issue (2014)

Temperature Abuse: One shipment was inadvertantly stored refrigerated rather than the labeled room temperature recommendation at McKesson Medical-Surgical Inc., one of the distributing wholesalers.

Class IIModerate

FDASep 12, 2014IN, MT, OR +1 more• Mckesson