Recalls / Class II
Class IID-0446-2024
Product
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.
- Affected lot / code info
- Lot #: H22212-FSV, Exp: 11/21/2024 1.0 kg pack size.
Why it was recalled
Failed Stability Specifications
Recalling firm
- Firm
- Specialty Process Labs LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 1850 E Riverview Dr, Phoenix, Arizona 85034-6703
Distribution
- Quantity
- 26 units
- Distribution pattern
- U.S. Nationwide.
Timeline
- Recall initiated
- 2024-03-01
- FDA classified
- 2024-04-17
- Posted by FDA
- 2024-04-24
- Status
- Completed
Source: openFDA Drug Enforcement endpoint. Recall record D-0446-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.