← FDA ENFORCEMENT
D-0294-2026Class II

Specialty Process Labs LLC

Recalling firm
Specialty Process Labs LLC
Product type
Drug
Status
Ongoing
Report date
2026-01-28
Distribution
U.S. Nationwide
Firm state
AZ
Product quantity
58 gms
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

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

Code / lot info

Lot #H22254-1XV; Exp. 01/31/2027

Other recalls SPEQ maps to Validation & Qualification
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See all Validation & Qualification recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.