FDA Drug Recalls

Recalls / Class II

Class IID-0294-2026

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

Affected lot / code info
Lot #H22254-1XV; Exp. 01/31/2027

Why it was recalled

Subpotent Drug

Recalling firm

Firm
Specialty Process Labs LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2001 W Lone Cactus Dr Ste B, Phoenix, Arizona 85027-2648

Distribution

Quantity
58 gms
Distribution pattern
U.S. Nationwide

Timeline

Recall initiated
2026-01-16
FDA classified
2026-01-21
Posted by FDA
2026-01-28
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0294-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.