FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

RLC Labs Nature-Throid Recall

Nature-Throid, Thyroid USP [liothyronine (T3) 22

RLC Labs Inc. · Phoenix, AZ

Risk level
Class II
Reported by FDA
Sep 23, 2020
Recall ID
D-1604-2020
Check your lot numberHow we source this data

Summary

RLC Labs recalled Nature-Throid starting Aug 25, 2020. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1604-2020 on Sep 23, 2020. Reason: CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Status: Terminated.

Why it was recalled

CGMP Deviations: manufactured under the same conditions as those found to be subpotent.

Product description

Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain (162.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3310-4; b) 60-count bottles, NDC 64727-3310-5; c) 90-count bottles, NDC 64727-3310-6; d) 100-count bottles, NDC 64727-3310-1; and e) 1,000-count bottles, NDC 64727-3310-2; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034.

Lot numbers, UPCs & expiration codes

All lots with expiry between 10/2020-07/2023

Where it was sold

Nationwide in the United States

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-1604-2020
Classification
Class II
Status
Terminated
Recall initiated
Aug 25, 2020
FDA report date
Sep 23, 2020
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
RLC Labs Inc.

Original FDA data

Every field from FDA enforcement report D-1604-2020, exactly as published.

Show all FDA fields
City
Phoenix
State
AZ
Status
Terminated
Country
United States
Event ID
86343
Address
1850 E Riverview Dr
Code information
All lots with expiry between 10/2020-07/2023
Postal code
85034-6703
Report date
Sep 23, 2020
Product type
Drugs
Recall number
D-1604-2020
Classification
Class II
Recalling firm
RLC Labs Inc.
Termination date
Nov 8, 2023
Reason for recall
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain (162.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3310-4; b) 60-count bottles, NDC 64727-3310-5; c) 90-count bottles, NDC 64727-3310-6; d) 100-count bottles, NDC 64727-3310-1; and e) 1,000-count bottles, NDC 64727-3310-2; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034.
Distribution pattern
Nationwide in the United States
Recall initiation date
Aug 25, 2020
Initial firm notification
E-Mail
Center classification date
Sep 24, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1604-2020, published Sep 23, 2020. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls