Warning
Specialty Process Labs LLC Recalls Thyroid
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0294-2026Drug / Pharmaceutical
Specialty Process Labs LLC Recalls Thyroid
Specialty Process Labs LLC · Class II — Moderate Risk
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
Reason for Recall
Subpotent Drug
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
U.S. Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the pharmaceutical product may cause temporary health problems or poses a slight threat of a serious nature. Specialty Process Labs LLC initiated the recall on January 16, 2026 affecting 58 gms. Subpotent Drug. The product was distributed in U.S. Nationwide. Consumers should check their purchases and discontinue use of any affected product. Contact Specialty Process Labs LLC for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.