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.