FDAClass IIFebruary 28, 2024

Adrenalin recall: Labeling Error

Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314…

Why was Adrenalin recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314…
Recalling firm
Henry Schein Inc. and Glove Club HSI Gloves Inc.
Quantity
1,099 Single Dose Vials
Distribution
USA nationwide.
Recall date
February 28, 2024
Classification
Class II
Status
Completed
Agency
FDA (drug)
Open FDA enforcement record Latest recalls