Adrenalin — Class II drug recall D-0342-2024
Completed recall by Henry Schein Inc. and Glove Club HSI Gloves Inc., reported 2024-02-28, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is in
| Recall number | D-0342-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Henry Schein Inc. and Glove Club HSI Gloves Inc., Melville, NY, United States |
| Recall initiated | 2024-01-17 |
| Classified | 2024-02-21 |
| Reported by FDA | 2024-02-28 |
| Distributed | Nationwide (US) |
| Quantity | 1,099 single |
| Reason classes | labeling |
| NDC | 00404-9810, 00404-9810-01, 42023-0159, 42023-0159-01, 42023-0159-25, 42023-0168, 42023-0168-01 |
| Lot numbers | 01/26, 11/24, 39747, 64103 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0342-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.