Drugs & medicalClass II

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…

cGMP Deviations: Products were stored outside the drug label specifications.

Read the official notice →
Date
2024-03-20
Country
United States
Brand
Mckesson Medical-Surgical Inc. Corporate Office
Product
Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC…
Classification
Class II
Units
Product was distributed to three direct accounts in NM, AZ and UT.
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Mckesson Medical-Surgical Inc. Corporate Office recalls

  1. 2024-10-02
  2. US
    Drugs & medicalClass II

    Mckesson Medical-Surgical Inc. Corporate Office recalls Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb,…

    Temperature abuse: Products exposed to improper temperature above drug label specifications.

    FDA · DrugMckesson Medical-Surgical Inc. Corporate OfficeProduct was distributed to two medical facilities in MD and VA.Official notice →
  3. 2024-06-19
  4. US
    Drugs & medicalClass II

    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…

    Quarantined product was inadvertently distributed

    FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution in the state of NJ.Official notice →
  5. 2024-03-27
  6. US
    Drugs & medicalClass II

    Mckesson Medical-Surgical Inc. Corporate Office recalls Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

    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…

    FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution in the states of AZ, PA and TX.Official notice →
  7. 2022-10-05
  8. US
    Drugs & medicalClass III

    Mckesson Medical-Surgical Inc. Corporate Office recalls SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll Ethylene Oxide (EO) Gas / Steam 3 Inch X…

    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.

    FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution.Official notice →
  9. 2022-08-31
  10. US
  11. US
    Drugs & medicalClass II

    Mckesson Medical-Surgical Inc. Corporate Office recalls a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood…

    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.

    FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS NationwideOfficial notice →
All 15 Mckesson Medical-Surgical Inc. Corporate Office recalls →

Other drugs & medical recalls in the United States

  1. 2024-03-20
  2. US
    Drugs & medicalClass II

    Eugia US LLC recalls Tobramycin for Injection, USP, 1.2 grams per Pharmacy Bulk Package, Rx Only, For Intravenous Use, PHARMACY BULK PACKAGE NOT FOR DIRECT…

    Failed Stability Specification: Water determination was found not complying with specification.

    FDA · DrugEugia US LLCNationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Optikem International, Inc. recalls TRP Natural Eyes Floaters Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane,…

    Lack of Assurance of Sterility

    FDA · DrugOptikem International, Inc.Product distributed Nationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    Thea Pharma, Inc. recalls Betimol (timolol ophthalmic solution) 0.5%, 15mL bottles, Rx only, Manufactured for: Thea Pharma Inc. Lexington, MA 02420, NDC 82584-002-15

    Lack of Assurance of Sterility: Out of specification for volume and compromised container closure.

    FDA · DrugThea Pharma, Inc.Product was distributed nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass II

    B. Braun Medical Inc recalls Potassium Chloride for Injection Concentrate USP, 500 mEq/250 mL (2 mEq/mL), 250 mL Bag, Rx only, B. Braun Medical Inc., Bethlehem, PA…

    Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.

    FDA · DrugB. Braun Medical IncNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Febuxostat Tablets 80mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN 38141,…

    CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
  7. 2024-03-13
  8. US
    Drugs & medicalClass II

    ConvaTec, Inc recalls ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System, REF 416938, 1 3/4 in. 45mm, Sterile.

    The kit contains a flange that has a 45mm coupling ring, however, the pouch within the kit is for a 57mm coupling ring.

    FDA · DeviceConvaTec, IncDistribution was made to AK, CA, FL, IL, IN, MI, NE, NJ, NY, OH, PA, and TX.…Official notice →
See all drugs & medical recalls →