Why it was recalled
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.
Lot numbers, UPCs & expiration codes
Lot #: H22212-FSV, Exp: 11/21/2024 1.0 kg pack size.
Where it was sold
U.S. Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0446-2024
- Classification
- Class II
- Status
- Completed
- Recall initiated
- Mar 1, 2024
- FDA report date
- Apr 24, 2024
- Quantity
- 26 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Specialty Process Labs LLC
Original FDA data
Every field from FDA enforcement report D-0446-2024, exactly as published.
Show all FDA fields
- City
- Phoenix
- State
- AZ
- Status
- Completed
- Country
- United States
- Event ID
- 94268
- Address
- 1850 E Riverview Dr
- Code information
- Lot #: H22212-FSV, Exp: 11/21/2024 1.0 kg pack size.
- Postal code
- 85034-6703
- Report date
- Apr 24, 2024
- Product type
- Drugs
- Recall number
- D-0446-2024
- Classification
- Class II
- Recalling firm
- Specialty Process Labs LLC
- Product quantity
- 26 units
- Reason for recall
- Failed Stability Specifications
- Voluntary / mandated
- Voluntary: Firm initiated
- 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.
- Recall initiation date
- Mar 1, 2024
- Initial firm notification
- Letter
- Center classification date
- Apr 17, 2024