← FDA ENFORCEMENT
D-0342-2024Class II

Henry Schein Inc. and Glove Club HSI Gloves Inc.

Recalling firm
Henry Schein Inc. and Glove Club HSI Gloves Inc.
Product type
Drug
Status
Completed
Report date
2024-02-28
Distribution
USA nationwide.
Firm state
NY
Product quantity
1,099 Single Dose Vials
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

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

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

Code / lot info

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

Other recalls SPEQ maps to Validation & Qualification
2026-07-22Class IIBell Pharmaceuticals, Inc2026-07-22Class IIBell Pharmaceuticals, Inc2026-07-22Class IIBell Pharmaceuticals, Inc2026-07-22Class IIBell Pharmaceuticals, Inc
See all Validation & Qualification recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.