🔍 RecallPedia

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

Class I - Dangerous
💊 Drugs Recalled: January 17, 2024 Henry Schein Inc. and Glove Club HSI Gloves Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Henry Schein Inc. and Glove Club HSI Gloves Inc.
Reason for Recall:
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
completed

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0342-2024