RLC Labs Recalls Subpotent Nature Throid Thyroid Medication
RLC Labs Inc. is recalling Nature Throid thyroid medication because FDA analysis found the product to be subpotent.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 according to the rubric.
Plain-English summary
RLC Labs Inc. is recalling Nature Throid, 3/4 Grain (48.75 mg) Thyroid USP, a prescription-only medication containing Liothyronine (T3) and Levothyroxine (T4). The recall affects 100-count and 1000-count bottles manufactured by RLC Labs in Phoenix, Arizona.
The recall was initiated because FDA analysis determined that the product is subpotent, meaning it does not contain the full amount of active ingredient required by the United States Pharmacopeia (USP). The specific lot number is 109242, with an expiration date of 11/2022.
The product was distributed nationwide in the United States. Patients and healthcare providers should stop using the affected medication and contact their healthcare provider for guidance on alternative treatment options.
The recalled product
- Product
- Nature Throid, 3/4 Grain (48.75 mg) Thyroid USP [Liothyronine (T3) 6.75 mcg, Levothyroxine (T4) 28.5 mcg], packaged in a) 100-count bottles (NDC 64727-3302-1) and b) 1000-count bottles (NDC 64727-3302-2), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034
- Manufacturer
- RLC Labs Inc.
- Category
- Drug — Thyroid Medication
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot #: 109242
- Exp. Date 11/2022
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 24 recalled by RLC Labs Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 24 products in this recall →Related recalls
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