Why it was recalled
CGMP Deviations
Product description
Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. (65mg)/Liothyronine (T3) 9mcg/Levothyroxine (T4) 38mcg, packaged in a) 90-count bottles (NDC 68788-7604-09), b) 100-count tablets (NDC 68788-7604-01), Rx Only, Mfg: RLC Labs; Cave Creek, AZ, Preferred Pharmaceuticals, Inc.
Lot numbers, UPCs & expiration codes
a) Lot #: A0220Q, Exp. Date: 10/31/2020; b) Lot #: K15171, Exp. Date: 10/31/2020
Where it was sold
Repackaged tablets sold to three physicians located in CA and GA.
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-1623-2020
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Sep 2, 2020
- FDA report date
- Sep 30, 2020
- Quantity
- N/A
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Preferred Pharmaceuticals, Inc.
Original FDA data
Every field from FDA enforcement report D-1623-2020, exactly as published.
Show all FDA fields
- City
- Anaheim
- State
- CA
- Status
- Terminated
- Country
- United States
- Event ID
- 86394
- Address
- 1250 N Lakeview Ave Ste O
- Code information
- a) Lot #: A0220Q, Exp. Date: 10/31/2020; b) Lot #: K15171, Exp. Date: 10/31/2020
- Postal code
- 92807-1801
- Report date
- Sep 30, 2020
- Product type
- Drugs
- Recall number
- D-1623-2020
- Classification
- Class II
- Recalling firm
- Preferred Pharmaceuticals, Inc.
- Termination date
- Apr 25, 2024
- Reason for recall
- CGMP Deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. (65mg)/Liothyronine (T3) 9mcg/Levothyroxine (T4) 38mcg, packaged in a) 90-count bottles (NDC 68788-7604-09), b) 100-count tablets (NDC 68788-7604-01), Rx Only, Mfg: RLC Labs; Cave Creek, AZ, Preferred Pharmaceuticals, Inc.
- Distribution pattern
- Repackaged tablets sold to three physicians located in CA and GA.
- Recall initiation date
- Sep 2, 2020
- Initial firm notification
- Letter
- Center classification date
- Sep 24, 2020