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FDAFDA · Food and drugs·Recall number D-0342-2024

Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314, Original NDC 42023-159-25 Repack NDC 0404-9810-01

Published February 28, 2024 · Recall initiated: January 17, 2024

Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
ADRENALIN
Manufacturer
Henry Schein Inc. and Glove Club HSI Gloves Inc.
Distributor
USA nationwide.
Lot
Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26
Risk classification
Class II
Area (FDA)
drug
Country
United States

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