RecallRadar

FDA Drug recall D-439-2013

Lloyd Thyro-Tab 0.112 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the labe…

On 2013-05-29 the FDA classified a Class II recall of Lloyd Thyro-Tab 0.112 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the labe… by Lloyd, citing cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-439-2013
ClassificationClass II
Statusterminated
Initiated2013-04-01
Published2013-05-29
Last updated2026-09-13 11:51 UTC
CompanyLloyd
DistributionUS

Product

Lloyd Thyro-Tab 0.112 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Reason

cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.

Identifiers

code_infoLot #: HE27211, Exp Apr-13; HE35511, Exp Jul-13; HA04112, Exp Aug-13; HC06212, Exp Sep-12.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-439-2013%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.