thejoe Mckesson Medical-Surgical Inc. Corpora

Mckesson Medical-Surgical Inc. Corporate Office: 157 FDA recall reports

Every drug recall the FDA has published for Mckesson Medical-Surgical Inc. Corporate Office. The fault, and how the agency graded it.

157Reports

0Class I

5Ongoing

2025-07-30Most recent

What the classes mean

The FDA sorts every recall into one of three classes. The class is the whole story. It is also the part people skip.

Class	What the FDA is saying
Class I	There is a reasonable probability that using this will cause serious harm or death.
Class II	It may cause temporary or reversible harm. Serious harm is unlikely.
Class III	It breaks a rule but is unlikely to hurt anyone. Often a labelling fault.

Class II is the bulk of every list here. That matters. A long list of Class II says something different from one Class I.

By class

Class	Reports
Class II	156
Class III	1

By year reported

Year	Reports
2022	147
2024	5
2025	5

Checking whether it affects you

The lot or code number is what matters. Not the product name. A recall covers specific lots. Yours may not be one of them.

Check the code on your package against the report. The FDA keeps the current list at fda.gov/safety/recalls.

The reports

The text below is quoted from the FDA record word for word.

EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Am

D-0539-2025 · Class II · reported 2025-07-30 · Ongoing

Why it was recalled: CGMP Deviations; potential temperature excursions due to transit delays
Product: 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.
Where it went: Within the U.S - OH, VA, FL.
How much: 2 Pre-filled syringes

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

D-0540-2025 · Class II · reported 2025-07-30 · Ongoing

Why it was recalled: CGMP Deviations; potential temperature excursions due to transit delays
Product: BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Where it went: Within the U.S - OH, VA, FL.
How much: 3 Vials

PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thous

D-0538-2025 · Class II · reported 2025-07-30 · Ongoing

Why it was recalled: CGMP Deviations; potential temperature excursions due to transit delays
Product: PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21
Where it went: Within the U.S - OH, VA, FL.
How much: 6 Pre-filled syringes

Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only,

D-0401-2025 · Class II · reported 2025-05-07 · Ongoing

Why it was recalled: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
Product: 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
Where it went: Distributed to Medical Facilities in MS and FL.
How much: 15

Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in I

D-0400-2025 · Class II · reported 2025-05-07 · Ongoing

Why it was recalled: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
Product: 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
Where it went: Distributed to Medical Facilities in MS and FL.
How much: 3

Hylenex recombinant (hyaluronidase) injection, 150 USP units/mL, 4x1 mL Single Dose Vials, Rx only, Manufactur

D-0116-2025 · Class II · reported 2024-12-18 · Terminated

Why it was recalled: cGMP Deviations: Temperature excursion
Product: 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
Where it went: Virgina
How much: 5 cartons/20 units each carton

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

D-0661-2024 · Class II · reported 2024-10-02 · Terminated

Why it was recalled: Temperature abuse: Products exposed to improper temperature above drug label specifications.
Product: Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
Where it went: Product was distributed to two medical facilities in MD and VA.
How much: 27 bottles

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

D-0373-2024 · Class II · reported 2024-03-20 · Terminated

Why it was recalled: cGMP Deviations: Products were stored outside the drug label specifications.
Product: 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
Where it went: Product was distributed to three direct accounts in NM, AZ and UT.
How much: 70 vials

Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedic

D-0371-2024 · Class II · reported 2024-03-20 · Terminated

Why it was recalled: cGMP Deviations: Products were stored outside the drug label specifications.
Product: Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10
Where it went: Product was distributed to three direct accounts in NM, AZ and UT.
How much: 70 vials

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

D-0372-2024 · Class II · reported 2024-03-20 · Terminated

Why it was recalled: cGMP Deviations: Products were stored outside the drug label specifications.
Product: Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01
Where it went: Product was distributed to three direct accounts in NM, AZ and UT.
How much: 70 vials

Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye drops, Eye Itch Relief, up t

D-1317-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye drops, Eye Itch Relief, up to 12 Hours, Sterile, 30 day supply, 5mL (0.17 FL OZ) bottle per box, Alcon, NDC 0065-4011-05.
Where it went: Nationwide in the USA.
How much: 9 boxes

Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%, Antihistamine, Eye Allergy Itc

D-1321-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%, Antihistamine, Eye Allergy Itch Relief, Once Daily, Sterile, 2.5 mL (0.085 FL OZ) bottle per box, Alcon, NDC 0065-8150-01.
Where it went: Nationwide in the USA.
How much: 1 box

Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ

D-1319-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g) bottle, Bayer Healthcare Pharmaceuticals, NDC 11523-7234-4.
Where it went: Nationwide in the USA.
How much: 67 bottles

Racepinephrine Inhalation Solution, USP 2.25%, Bronchodilator, For Oral Inhalation Only, Sulfite Free, Preserv

D-1325-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Racepinephrine Inhalation Solution, USP 2.25%, Bronchodilator, For Oral Inhalation Only, Sulfite Free, Preservative Free, 30 x 0.5 mL Sterile Unit-of-Use Vials, each in a foil pouch, per carton, Nephron Pharmaceuticals Corporation, NDC 0487-5901-99.
Where it went: Nationwide in the USA.
How much: 23 cartons

GenTeal Tears, Lubricant Eye Ointment, Night-Time Ointment, Sterile, 3.5 gm (0.12 FL OZ) per box, Alcon, NDC 0

D-1320-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: GenTeal Tears, Lubricant Eye Ointment, Night-Time Ointment, Sterile, 3.5 gm (0.12 FL OZ) per box, Alcon, NDC 0065-0518-01.
Where it went: Nationwide in the USA.
How much: 40 boxes

Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of inte

D-1324-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.
Where it went: Nationwide in the USA.
How much: 1 box

Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC 0436-0672-16, b) sodium hypochlorite 0.

D-1323-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC 0436-0672-16, b) sodium hypochlorite 0.25%, half strength, NDC 0436-0936-16, c) sodium hypochlorite 0.5% full strength, NDC 0436-0946-16, Antimicrobial, 473 mL (16 fl oz) bottle, Century Pharmaceuticals, Inc.
Where it went: Nationwide in the USA.
How much: 113 bottles

Alcohol Swabsticks, Antiseptic, 50 4" saturated individual packets per box, Manufactured for: Dynarex Corporat

D-1327-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Alcohol Swabsticks, Antiseptic, 50 4" saturated individual packets per box, Manufactured for: Dynarex Corporation, NY 10962, Made in Mexico, NDC 67777-300-01 (current NDC) NDC# 67777-120-10 (discontinued)
Where it went: Nationwide in the USA.

Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.

D-1315-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.
Where it went: Nationwide in the USA.
How much: 16 boxes

Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Trip

D-1311-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Triple Antibiotic Ointment, 144 packets per box, Net wt. per packet 0.5 g, Honeywell Safety Products, NDC 0498-0750-36.
Where it went: Nationwide in the USA.
How much: 6 boxes

Naphcon A eye drops, Naphazoline HCl 0.025% and Pheniramine Maleate 0.3%, Redness Reliever and Antihistamine E

D-1313-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Naphcon A eye drops, Naphazoline HCl 0.025% and Pheniramine Maleate 0.3%, Redness Reliever and Antihistamine Eye Drops, Sterile, 15 mL (0.5 FL OZ) bottle per box, Alcon, a Novartis company, NDC 0065-0085-15.
Where it went: Nationwide in the USA.
How much: 12 boxes

Bisacodyl Suppositories, Fast Acting Stimulant Laxative, 100 suppositories per box, 10 mg each, Health Star, N

D-1312-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Bisacodyl Suppositories, Fast Acting Stimulant Laxative, 100 suppositories per box, 10 mg each, Health Star, NDC 57896-443-01.
Where it went: Nationwide in the USA.
How much: 45 boxes

Systane, Lubricant Eye Drops, Polyethylene Glycol 400 0.4% Lubricant, Propylene Glycol 0.3% Lubricant, Origina

D-1314-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Systane, Lubricant Eye Drops, Polyethylene Glycol 400 0.4% Lubricant, Propylene Glycol 0.3% Lubricant, Original, Long Lasting Dry Eye Relief, Sterile, a) 15 mL (0.5 FL OZ) NDC 0065-0429-15, b) 30 mL (1 FL OZ) NDC 0065-0429-30, bottle per box, Alcon Surgical Inc.
Where it went: Nationwide in the USA.
How much: 47 bottles

Systane Balance, Lubricant Eye Drops, Propylene Glycol 0.6% lubricant, Restorative Formula, Sterile, 10 mL (1/

D-1316-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Systane Balance, Lubricant Eye Drops, Propylene Glycol 0.6% lubricant, Restorative Formula, Sterile, 10 mL (1/3 FL OZ) bottle per box, Alcon, NDC 0065-1433-02.
Where it went: Nationwide in the USA.
How much: 12 boxes

Debrox, Carbamide Peroxide, Earwax Removal Aid, 0.5 FL OZ (15 mL) bottle per box), MedTech Products Inc., NDC

D-1318-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Debrox, Carbamide Peroxide, Earwax Removal Aid, 0.5 FL OZ (15 mL) bottle per box), MedTech Products Inc., NDC 63029-321-01.
Where it went: Nationwide in the USA.
How much: 131 boxes

A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC

D-1322-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.
Where it went: Nationwide in the USA.
How much: 1 Jar

Sterile Alcohol Prep Pads, Sterile, Latex Free, 100 large pads per box, manufactured for: Dynarex Corporation,

D-1326-2022 · Class II · reported 2022-08-17 · Terminated

Why it was recalled: CGMP Deviations: products were stored outside the drug label specifications.
Product: Sterile Alcohol Prep Pads, Sterile, Latex Free, 100 large pads per box, manufactured for: Dynarex Corporation, NY 10962, NDC 67777-121-16.
Where it went: Nationwide in the USA.
How much: 10 boxes

Thrombin JMI, Vial 5,000IU 2/diluent, kit, Rx only, MFG: Pfizer NDC 60793-215-05

D-1099-2022 · Class II · reported 2022-06-15 · Terminated

Why it was recalled: cGMP deviations: Temperature abuse
Product: Thrombin JMI, Vial 5,000IU 2/diluent, kit, Rx only, MFG: Pfizer NDC 60793-215-05
Where it went: USA nationwide.
How much: 157 kits

Cefazolin for injection USP, and Dextrose Injection, USP, 2 g, 50 mL duplex container, Rx only, MFG: B. Braun

D-1118-2022 · Class II · reported 2022-06-15 · Terminated

Why it was recalled: cGMP deviations: Temperature abuse
Product: Cefazolin for injection USP, and Dextrose Injection, USP, 2 g, 50 mL duplex container, Rx only, MFG: B. Braun Medical Inc., NDC 0264-3105-11
Where it went: USA nationwide.
How much: 39 cases

Duraclon (clonidine HCl injection, USP), 1000 mcg/10 mL (100 mcg/mL), 10 mL single-dose vial, Rx only, MFG: My

D-1091-2022 · Class II · reported 2022-06-15 · Terminated

Why it was recalled: cGMP deviations: Temperature abuse
Product: Duraclon (clonidine HCl injection, USP), 1000 mcg/10 mL (100 mcg/mL), 10 mL single-dose vial, Rx only, MFG: Mylan Pharma, NDC 67457-218-10
Where it went: USA nationwide.
How much: 9 vials

Showing the 30 most recent of 157. The rest are searchable at the FDA enforcement report database.

Read these counts with three things in mind

A firm with more recalls usually makes more products. A contract packer runs hundreds of lines. It will out-recall a company with one product whatever either does. This is not a safety ranking.

Most recalls here are voluntary. A firm found its own fault and pulled the stock. That is the system working. It lands in this database looking the same as a recall the FDA had to push for.

Terminated means the FDA considers the recall finished. It is not a verdict. It does not mean anyone was harmed.

Source: openFDA enforcement reports, retrieved 2026-08-05. FDA dataset last updated 2026-07-29.

← All drug recalls