Recall Atlas
Drugs & medicalClass II

Henry Schein Inc. and Glove Club HSI Gloves Inc. recalls Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80…

Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.

Read the official notice →
Date
2024-02-28
Country
United States
Brand
Henry Schein Inc. and Glove Club HSI Gloves Inc.
Product
Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA…
Classification
Class II
Units
USA nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2024-02-28
  2. US
    Drugs & medicalClass I

    Insight Pharmaceuticals LLC, a Prestige Consumer… recalls TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by:…

    Chemical Contamination; presence of benzene.

    FDA · DrugInsight Pharmaceuticals LLC, a Prestige Consumer…Product was distributed nationwide and to 4 foreign accounts. Guaynabo, Puerto…Official notice →
  3. US
    Drugs & medicalClass I

    Today The World recalls Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001,…

    Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this…

    FDA · DrugToday The WorldProduct distributed nationwide within the United States.Official notice →
  4. US
    Drugs & medicalClass I

    Today The World recalls Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada

    Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this…

    FDA · DrugToday The WorldProduct distributed nationwide within the United States.Official notice →
  5. US
    Drugs & medicalClass II

    Mallinckrodt Hospital Products Inc. recalls Terlivaz (terlipressin for injection), 0.85mg/vial, Single-Dose Vial, Rx only, Distributed by: Mallinckrodt Hospital…

    cGMP deviations: Temperature excursion due to shipping delay from manufacturer to distributor. Affected distributor has been notified.

    FDA · DrugMallinckrodt Hospital Products Inc.USA nationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    Ascend Laboratories, LLC recalls Fosfomycin Tromethamine Granules for Oral Solution, (equivalent to 3 grams of fosfomycin), single-dose sachet, Rx Only, Manufactured by:…

    Failed Impurities/Degradation Specification: Out of specification for organic impurities

    FDA · DrugAscend Laboratories, LLCNationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass II

    Alpha Aromatics recalls Pure Care Foaming Mint Hand Sanitizer 62%, Distributed by: Air Scent International, 290 Alpha Drive, RIDC Industrial Park, Pittsburg, PA…

    CGMP Deviations

    FDA · DrugAlpha AromaticsProduct was distributed to two accounts in NC and MIOfficial notice →
See all drugs & medical recalls →