Drugs & medicalClass I

McKesson recalls UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041…

Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.

Read the official notice →
Date
2026-02-18
Country
United States
Brand
McKesson
Product
UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041…
Classification
Class I
Units
Nationwide in the USA
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 Details may be shortened or out of date; the official notice is the authoritative source.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 recalls

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    McKesson recalls Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only, Manufactured by:…

    Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.

    FDA · DrugMcKessonNationwide within the United StatesOfficial notice →
  3. 2025-02-05
  4. US
    Drugs & medicalClass II

    McKesson recalls Inflectra (infliximab-dyyb), For injection, 100mg per vial, packaged in 10 mL single-dose vial, Rx only, Mfd by: CELLTRION, INC, Dist. by:…

    cGMP Deviations: Product intended for quarantine was inadvertently distributed.

    FDA · DrugMcKessonNationwide USAOfficial notice →
  5. 2024-02-28
  6. US
    Drugs & medicalClass II

    MCKESSON CORPORATION recalls CABTREO (clindamycin phosphate, adapalene and benzoyl peroxide) Topical Gel 1.2%/0.15%/3.1%, Not for Oral, Ophthalmic or Intravaginal Use,…

    CGMP Deviations: Product was stored outside labeled storage temperature requirements. Product was exposed to controlled room temperature environment instead of remaining refrigerated.

    FDA · DrugMCKESSON CORPORATIONNationwide in the USOfficial notice →
All 4 McKesson recalls →

Other drugs & medical recalls in the United States

  1. 2026-02-18
  2. US
    Drugs & medicalClass II

    Philips North America Llc recalls Brilliance iCT; Product Code (REF): 728306;

    As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners…

    FDA · DevicePhilips North America LlcWorldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT,…Official notice →
  3. US
    Drugs & medicalClass II

    Hologic, Inc recalls Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.

    Presence of particulates in affected devices that can be deposited into breast tissue during use.

    FDA · DeviceHologic, IncUS Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit

    A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory…

    FDA · DeviceMedline Industries, LPDistribution US nationwide and Canada.Official notice →
  5. US
    Drugs & medicalClass II

    Meitheal Pharmaceuticals, Inc recalls Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago,…

    Defective Delivery System: Missing or duplicated needles within the injection kit

    FDA · DrugMeitheal Pharmaceuticals, IncU.S. NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product…

    Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

    FDA · DrugAmerisource Health Services LLCNationwide in the USAOfficial notice →
  7. US
See all drugs & medical recalls →