FDA Recall D-0392-2026
New Life Pharma LLC · Northvale, NJ
Class II Ongoing 77 days on record
Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.
Product
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.
Reason for recall
Lack of Assurance of Sterility
Recall record
- Recall number
D-0392-2026- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Letter
- Distribution
- OH
- Recall initiated
- 2026-02-26
- Classified by FDA Center
- 2026-03-17
- FDA published
- 2026-03-11
- Recalling firm
- New Life Pharma LLC
- Firm location
- Northvale, NJ
Operational response
Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.
For the official FDA enforcement record, see FDA's Recall Search.