← FDA ENFORCEMENT
D-0446-2024Class II

Specialty Process Labs LLC

Recalling firm
Specialty Process Labs LLC
Product type
Drug
Status
Completed
Report date
2024-04-24
Distribution
U.S. Nationwide.
Firm state
AZ
Product quantity
26 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

Failed Stability Specifications

Product description

S.P.Labs, Thyroid, Full Strength, Rx only, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-500-01.

Code / lot info

Lot #: H22212-FSV, Exp: 11/21/2024 1.0 kg pack size.

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.