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
Reported: February 28, 2024 Initiated: January 17, 2024 #D-0342-2024
Product 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
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Details
- Recalling Firm
- Henry Schein Inc. and Glove Club HSI Gloves Inc.
- Units Affected
- 1,099 Single Dose Vials
- Distribution
- USA nationwide.
- Location
- Melville, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Henry Schein Inc. and Glove Club HSI Gloves Inc.. Units affected: 1,099 Single Dose Vials.
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 28, 2024. Severity: Moderate. Recall number: D-0342-2024.
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