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

FDA recall notice · announced February 28, 2024 · Henry Schein Inc. And Glove Club Hsi Gloves

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

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

Reason for recall

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

Notes

Distribution: USA nationwide.
Lot/code information: Original Lot # 64103, exp. date 11/24 Repackaged Lot # 39747, exp. date 01/26
Quantity: 1,099 Single Dose Vials
Status: Completed
Products in this recall event:
- 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 (D-0342-2024)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.