FDA recall D-1598-2020

RLC Labs Inc. · Class II · drug

Product

Nature-Throid, Thyroid USP [liothyronine (T3) 4.5 mcg and levothyroxine (T4) 19 mcg], 1/2 Grain (32.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3299-4; b) 60-count bottles, NDC 64727-3299-5; c) 90-count bottles, NDC 64727-3299-6; d) 100-count bottles, NDC 64727-3299-1; and e) 1000-count bottles, NDC 64727-3299-2; 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.

Distribution

Nationwide in the United States

Key facts

Status
Terminated
Initiation date
2020-08-25
Report date
2020-09-23
Termination date
2023-11-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Phoenix, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1598-2020