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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