FDA Drug Recalls

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.

Class II recall: drug · FDA Drug Recalls