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.

Read the official notice →
Date
2024-10-02
Country
United States
Brand
Mckesson Medical-Surgical Inc. Corporate Office
Product
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
Classification
Class II
Units
Product was distributed to two medical facilities in MD and VA.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-05-07
  2. US
    Drugs & medicalClass II

    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,…

    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…

    FDA · DrugMckesson Medical-Surgical Inc. Corporate OfficeDistributed to Medical Facilities in MS and FL.Official notice →
  3. 2024-12-18
  4. US
  5. 2024-10-30
  6. US
    Drugs & medicalClass II

    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…

    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.

    FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution in the state of DC.Official notice →
  7. 2024-06-19
  8. 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 →
  9. 2024-03-27
  10. 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 →
  11. 2024-03-20
  12. US
    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.

    FDA · DrugMckesson Medical-Surgical Inc. Corporate OfficeProduct was distributed to three direct accounts in NM, AZ and UT.Official notice →
All 15 Mckesson Medical-Surgical Inc. Corporate Office recalls →

Other drugs & medical recalls in the United States

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

    AbbVie Inc. recalls Refresh P.M., (Mineral Oil 42.5%, White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allergen,…

    Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.

    FDA · DrugAbbVie Inc.Nationwide in the USA, Foreign Consignees (Austrailia, Canada, Great Britain)Official notice →
  3. US
  4. US
    Drugs & medicalClass II

    Vivier Pharma, Inc. recalls Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% and zinc oxide 8%) packaged in 60 ml/2 fl oz, Vivier Canada Inc. /…

    Microbial Contamination of Non-Sterile Product

    FDA · DrugVivier Pharma, Inc.Nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513,…

    Subpotent Drug

    FDA · DrugGlenmark Pharmaceuticals Inc., USAProduct was distributed nationwide within the United States.Official notice →
  6. 2024-09-25
  7. US
    Drugs & medicalClass II

    Unomedical A/S recalls VariSoft Infusion Set, Single Use.

    Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".

    FDA · DeviceUnomedical A/SUS Nationwide distribution in the state of California.Official notice →
  8. US
    Drugs & medicalClass II

    Cypress Medical Products LLC recalls BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025

    Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.

    FDA · DeviceCypress Medical Products LLCUS Nationwide distribution.Official notice →
See all drugs & medical recalls →