Thyroid — Class II drug recall D-0294-2026
Ongoing recall by Specialty Process Labs LLC, reported 2026-01-28, distributed nationwide. Subpotent Drug
| Recall number | D-0294-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Specialty Process Labs LLC, Phoenix, AZ, United States |
| Recall initiated | 2026-01-16 |
| Classified | 2026-01-21 |
| Reported by FDA | 2026-01-28 |
| Distributed | Nationwide (US) |
| Quantity | 58 gms |
| Reason classes | potency |
| NDC | 81305-0100-02 |
| Lot numbers | H22254-1XV |
| Expiration dates | 2027-01-31 |
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
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-0294-2026. 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.