WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30 Tablets, NDC 64727-5750-4; c) 60 Tablets, NDC 64727-5750-5; d) 90 Tablets, NDC 64727-5750-6; e) 100 Tablets, NDC 64727-5750-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034
Reported: September 23, 2020 Initiated: August 25, 2020 #D-1609-2020
Product Description
WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30 Tablets, NDC 64727-5750-4; c) 60 Tablets, NDC 64727-5750-5; d) 90 Tablets, NDC 64727-5750-6; e) 100 Tablets, NDC 64727-5750-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034
Reason for Recall
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Details
- Recalling Firm
- RLC Labs Inc.
- Units Affected
- N/A
- Distribution
- Nationwide in the United States
- Location
- Phoenix, AZ
Frequently Asked Questions
What product was recalled? ▼
WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30 Tablets, NDC 64727-5750-4; c) 60 Tablets, NDC 64727-5750-5; d) 90 Tablets, NDC 64727-5750-6; e) 100 Tablets, NDC 64727-5750-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034. Recalled by RLC Labs Inc.. Units affected: N/A.
Why was this product recalled? ▼
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 23, 2020. Severity: Moderate. Recall number: D-1609-2020.
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