Richmond, VA, United States
Mckesson Medical-Surgical Inc. Corporate Office recalls
15 recalls recorded since 2018, most recently on 30 July 2025. 8 are listed as ongoing. Status and classification are as published by the FDA.
Recalls15
Ongoing (FDA)8
Terminated or completed7
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 30 July 2025
- Reason
- Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.
- Distribution
- US Nationwide distribution in the state of Georgia.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2337-2025
- Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020
Ongoing Class II Drugs
- Recall started
- 25 April 2025
- Reason
- 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.
- Distribution
- Distributed to Medical Facilities in MS and FL.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-0401-2025, D-0400-2025
- 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, Dee
- 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
Ongoing Class II Medical devices
- Recall started
- 24 April 2025
- Reason
- transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
- Distribution
- US Nationwide distribution in the states of AL, AR, IL, KS, MT, NC, NJ, OR, SC, TN & WV.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1854-2025, Z-1846-2025, Z-1836-2025, Z-1837-2025, Z-1842-2025, Z-1851-2025, Z-1850-2025, Z-1843-2025, Z-1825-2025, Z-1855-2025, Z-1831-2025, Z-1840-2025 and 20 more
- SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.
- ABBOTT POINT OF CARE TEST CREA I-STAT (25/BX) ABBTPT CARTRIDGE.
- ORTHO CLINICAL DIAGNOSTICS INC ANTI-B BIOCLONE 10ML3X10ML.
- ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT.
- ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.
- ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.
- ABBOTT DIAGNOSTICS ARCHITECT FREE T4ABBDIA CALIBRATOR.
- ABBOTT DIAGNOSTICS ARC ANTI-TPO ASSAY 100TST B REAGENT.
- and 24 more product lines
Ongoing Class II Drugs
- Recall started
- 21 April 2025
- Reason
- CGMP Deviations; potential temperature excursions due to transit delays
- Distribution
- Within the U.S - OH, VA, FL.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-0539-2025, D-0540-2025, D-0538-2025
- 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.
- BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
- PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21
Ongoing Class II Medical devices
- Recall started
- 17 September 2024
- Reason
- The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the validated summer packaging and may have been exposed to temperatures above 25¿C. This may lead to delay in patients' results.
- Distribution
- US Nationwide distribution in the state of DC.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0138-2025
- 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.
Terminated Class II Drugs
- Recall started
- 11 September 2024
- Terminated
- 20 August 2025
- Reason
- cGMP Deviations: Temperature excursion
- Distribution
- Virgina
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0116-2025
- 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
Terminated Class II Drugs
- Recall started
- 11 September 2024
- Terminated
- 29 January 2025
- Reason
- Temperature abuse: Products exposed to improper temperature above drug label specifications.
- Distribution
- Product was distributed to two medical facilities in MD and VA.
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0661-2024
- Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
Completed Class II Medical devices
- Recall started
- 23 April 2024
- Reason
- Quarantined product was inadvertently distributed
- Distribution
- US Nationwide distribution in the state of NJ.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2039-2024
- 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
Terminated Class II Drugs
- Recall started
- 7 February 2024
- Terminated
- 14 August 2024
- Reason
- cGMP Deviations: Products were stored outside the drug label specifications.
- Distribution
- Product was distributed to three direct accounts in NM, AZ and UT.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-0373-2024, D-0371-2024, D-0372-2024
- 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
- Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10
- Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01
Ongoing Class II Medical devices
- Recall started
- 9 January 2024
- Reason
- Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.
- Distribution
- US Nationwide distribution in the states of AZ, PA and TX.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1313-2024, Z-1311-2024, Z-1314-2024, Z-1312-2024, Z-1315-2024
- Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
- Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis
- Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL
- Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 mL
- Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
Terminated Class II Drugs
- Recall started
- 29 June 2022
- Terminated
- 13 February 2024
- Reason
- CGMP Deviations: products were stored outside the drug label specifications.
- Distribution
- Nationwide in the USA.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-1317-2022, D-1321-2022, D-1319-2022, D-1325-2022, D-1320-2022, D-1324-2022, D-1323-2022, D-1327-2022, D-1315-2022, D-1311-2022, D-1313-2022, D-1312-2022 and 5 more
- 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.
- 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.
- 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.
- 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 C
- GenTeal Tears, Lubricant Eye Ointment, Night-Time Ointment, Sterile, 3.5 gm (0.12 FL OZ) per box, Alcon, NDC 0065-0518-01.
- 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 Pharmaceutica
- 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, Antimicrobi
- 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)
- and 9 more product lines
Ongoing Class II Medical devices
- Recall started
- 25 May 2022
- Reason
- Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
- Distribution
- US Nationwide
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1583-2022, Z-1636-2022, Z-1586-2022, Z-1615-2022, Z-1591-2022, Z-1596-2022, Z-1630-2022, Z-1629-2022, Z-1597-2022, Z-1620-2022, Z-1619-2022, Z-1599-2022 and 43 more
- a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50 Tests-IVD. Part No. 0356-50. b. Coagulation Control Kit Coag-Sense PT / INR Test (Prothrombin T
- FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712
- a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933
- MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047
- Perifix LOR Syringe Perifix 8 mL Pouch Luer Lock Tip Without Safety Model Number: 332152
- Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604
- CENTURION MEDICAL PRODUCTS, LP Centurion CATH KIT, FML W/LUBE 8FR (50/CS) CNTURN Catalog # CKF105L
- BECKMAN COULTER, INC. a. COULTER DxH Diff Pack REAGENT, DIFF PK FP DXHCOULTR, Catalog #628020. b. COULTER DxH Cleaner REAGENT, CLEANER FP DXH 10LCOULTR Catalog #628023. c. DxH 500 Series Lyse LYSE, VERSA SOL DX
- and 47 more product lines
Ongoing Class III Medical devices
- Recall started
- 25 May 2022
- Reason
- Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
- Distribution
- US Nationwide distribution.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1791-2022, Z-1803-2022, Z-1787-2022, Z-1790-2022, Z-1789-2022, Z-1801-2022, Z-1796-2022, Z-1807-2022, Z-1802-2022, Z-1794-2022, Z-1793-2022, Z-1795-2022 and 11 more
- SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll Ethylene Oxide (EO) Gas / Steam 3 Inch X 100 Foot Transparent / Blue Self Seal Paper / Film Model Number: SCT3.
- Absorbent dressings. a. DERMA SCIENCES, INC. McKesson PACKING STRIP, PLAIN 1/4"X5YDSSTR LF (12 MGM61 61- Catalog #61-59120. b. DERMA SCIENCES, INC. McKesson PACKING STRIP, PLAIN 1/2"X5YDSSTR LF (12/CS) MGM61 Catalog #61-
- DERMARITE INDUSTRIES SafeWash Saline Saline Wound Flush SafeWash 7.1 oz. Can Sterile 0.9% Sodium Chloride Model Number: 00245
- a. SporView Culture Set SporView Sterilization Biological Indicator Kit Steam / EO Gas / Dry Heat / Chemical Vapor Model Number: CS-020 b. SPORVIEW CULTURE SET SporView Sterilization Biological Indicator Kit Steam / E
- DERMARITE INDUSTRIES DermaCol 100 Collagen Powder DermaCol 100 Collagen 1 Gram Model Number: 00300E
- Skin markers: a. IZI MEDICAL PRODUCTS LLC Multi-Modality Markers SKIN MARKER RADIO 1.5MM 50BX Catalog #MM3005. b. SKIN MARKER MAMMO BB2.0 100B - Mammography Skin Marker Catalog # SDM-BB20.
- a. DERMARITE INDUSTRIES DermaCol Collagen Dressing DermaCol Without Border Collagen / Sodium Alginate / Carboxyl Methylcellulose (CMC) / Ethylenediamine-tetraacetic Acid (EDTA) 4 X 4 Inch 10 Count Model Number: 00303E.
- 3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158
- and 15 more product lines
Terminated Class II, Class III Drugs
- Recall started
- 13 April 2022
- Terminated
- 30 November 2023
- Reason
- cGMP deviations: Temperature abuse
- Distribution
- USA nationwide.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-1099-2022, D-1118-2022, D-1091-2022, D-1017-2022, D-1030-2022, D-1003-2022, D-1119-2022, D-1056-2022, D-1095-2022, D-1039-2022, D-1098-2022, D-1090-2022 and 118 more
- Thrombin JMI, Vial 5,000IU 2/diluent, kit, Rx only, MFG: Pfizer NDC 60793-215-05
- 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
- 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
- GlucaGen (glucagon) for injection, 1 mg per vial, single dose kit, Rx only, Manufactured for: Boehringer Mannheim, NDC 0597-0260-10
- Spinal Tray (A4058-25 Spinal Tray 25G Whitacre No Epinephrine), Rx only, Manufacturer: Smiths Medical ASD, Inc., NJ
- Dexmedetomidine HCL Single Dose Vial 200 mcg per 2 mL (100mcg/mL), Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0209-02
- Intralipid (I.V. Fat emulsion), 20%, 250 mL bag, Rx only, MFG: Baxter Healthcare, NDC 0338-0519-09
- Metronidazole tablets, USP 250 mg, 100-count unit dose box, Rx only, MFG: Major Pharma, NDC 0904-1453-61
- and 122 more product lines
Terminated Class II Medical devices
- Recall started
- 2 June 2021
- Terminated
- 28 April 2022
- Reason
- Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.
- Distribution
- US Nationwide Distribution
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2081-2021
- ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.