Home/Recalls/FDA-D-0392-2026
FDA DrugsClass II

Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Val...

Published: March 11, 2026Recall ID: D-0392-2026Category: drugsCountry: US

Reason for Recall / Hazard

Lack of Assurance of Sterility

Product Description & Identification

Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.

Additional Source Details

FieldValue
CityNorthvale
StateNJ
Event id98496
Address 1265 Livingston St
Address 2N/A
Code infoLot 241113, Exp Date 11/30/2026 & Lot 250103, Exp Date 1/31/2027
Postal code07647-1901
Report date20260311
Product typeDrugs
Product quantity820 vials
Reason for recallLack of Assurance of Sterility
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260226
Initial firm notificationLetter
Center classification date20260317

Overview

  • Recalling FirmNew Life Pharma LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionOH
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