FDAFDA · Food and drugs·Recall number D-1610-2020
WP Thyroid, Westhroid Pure, 1.25 Grain (81.25 mg) Thyroid USP packaged in a) 1,000 Tablets, NDC 64727-6050-2 ; b) 30 Tablets, NDC 64727-6050-4; c) 60 Tablets, NDC 64727-6050-5; d) 90 Tablets, NDC 64727-6050-6; e) 100 Tablets, NDC 64727-6050-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034
Published September 23, 2020 · Recall initiated: August 25, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- RLC Labs Inc.
- Distributor
- Nationwide in the United States
- Lot
- All lots with expiry between 10/2020-07/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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