WP Thyroid, Westhroid Pure, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], packaged in a) 30-count bottles (NDC 64727-5550-4), b) 90-count bottles (NDC 64727-5550-6), c) 100-count bottles (NDC 64727-5550-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024
Reported: September 23, 2020 Initiated: August 25, 2020 #D-1614-2020
Product Description
WP Thyroid, Westhroid Pure, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], packaged in a) 30-count bottles (NDC 64727-5550-4), b) 90-count bottles (NDC 64727-5550-6), c) 100-count bottles (NDC 64727-5550-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024
Reason for Recall
Subpotent Drug: FDA analysis found product 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, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], packaged in a) 30-count bottles (NDC 64727-5550-4), b) 90-count bottles (NDC 64727-5550-6), c) 100-count bottles (NDC 64727-5550-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024. Recalled by RLC Labs Inc.. Units affected: N/A.
Why was this product recalled? ▼
Subpotent Drug: FDA analysis found product to be subpotent
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 23, 2020. Severity: Critical. Recall number: D-1614-2020.
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