FDA Recall D-0294-2026
Specialty Process Labs LLC · Phoenix, AZ
Class II Ongoing 118 days on record
Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.
Product
Thyroid, USP, Rx only, Net Wt: 0.50kg, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-100-02
Reason for recall
Subpotent Drug
Recall record
- Recall number
D-0294-2026- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Letter
- Distribution
- U.S. Nationwide
- Recall initiated
- 2026-01-16
- Classified by FDA Center
- 2026-01-21
- FDA published
- 2026-01-28
- Recalling firm
- Specialty Process Labs LLC
- Firm location
- Phoenix, AZ
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.