Class I · High risk
Thyroid Tablets
Superpotent Drug
Thyroid
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Subpotent Drug
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
What was recalled
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 NDC
81305-0100-02
Compare with the code on your package — it is the most precise check available.
Drug: Thyroid Category: Thyroid Medication
- Recalling firm
- Specialty Process Labs LLC
- NDC code
- 81305-100-02
- Origin
- AZ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0294-2026 · FDA notice
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.
Other Thyroid recalls
See all
Class II · Moderate risk
S.P Labs
Failed Stability Specifications
Class II · Moderate risk
S.P.Labs
Failed Stability Specifications
Class II · Moderate risk
Levothyroxine 25mcg in Ns 1.25ml Syringe
Lack of sterility assurance
Class II · Moderate risk
Armour Thyroid
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Other recalls by Specialty Process Labs LLC
All 2026 recallsFree recall alerts
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