Why it was recalled
Subpotent Drug
Product description
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
Lot numbers, UPCs & expiration codes
Lot #H22254-1XV; Exp. 01/31/2027
Where it was sold
U.S. Nationwide
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0294-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jan 16, 2026
- FDA report date
- Jan 28, 2026
- Quantity
- 58 gms
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Specialty Process Labs LLC
Original FDA data
Every field from FDA enforcement report D-0294-2026, exactly as published.
Show all FDA fields
- City
- Phoenix
- State
- AZ
- Status
- Ongoing
- Country
- United States
- Event ID
- 98307
- Address
- 2001 W Lone Cactus Dr Ste B
- Code information
- Lot #H22254-1XV; Exp. 01/31/2027
- Postal code
- 85027-2648
- Report date
- Jan 28, 2026
- Product type
- Drugs
- Recall number
- D-0294-2026
- Classification
- Class II
- Recalling firm
- Specialty Process Labs LLC
- Product quantity
- 58 gms
- Reason for recall
- Subpotent Drug
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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
- Distribution pattern
- U.S. Nationwide
- Recall initiation date
- Jan 16, 2026
- Initial firm notification
- Letter
- Center classification date
- Jan 21, 2026