Specialty Process Labs LLC: Drug Recall

Recall #D-0446-2024 · 03/01/2024

Class II: Risk

Recall Details

Recall Number
D-0446-2024
Classification
Class II
Product Type
Drug
Recalling Firm
Specialty Process Labs LLC
Status
Completed
Date Initiated
03/01/2024
Location
Phoenix, AZ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
26 units

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.

Distribution Pattern

U.S. Nationwide.

Other Recalls by Specialty Process Labs LLC

View all recalls by Specialty Process Labs LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.