RecallRadar

FDA Drug recall D-1344-2014

Liothyronine Sodium Tablets, USP 5 mcg, Rx Only, a) 100-count bottle NDC 42794-018-02 and b) 1000-count bottle NDC 42794-018-06, SigmaPharm…

On 2014-05-28 the FDA classified a Class II recall of Liothyronine Sodium Tablets, USP 5 mcg, Rx Only, a) 100-count bottle NDC 42794-018-02 and b) 1000-count bottle NDC 42794-018-06, SigmaPharm… by Sigmapharm Laboratories, citing cross Contamination with Other Products: Four lots of Liothyronine Sodium Tablets, USP 5 mcg are being recalled due to the finding of a potential carryover of trace amounts of a p….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1344-2014
ClassificationClass II
Statusterminated
Initiated2014-04-22
Published2014-05-28
Last updated2026-09-13 11:51 UTC
CompanySigmapharm Laboratories
DistributionUS

Product

Liothyronine Sodium Tablets, USP 5 mcg, Rx Only, a) 100-count bottle NDC 42794-018-02 and b) 1000-count bottle NDC 42794-018-06, SigmaPharm Laboratories, LLC, Bensalem, Pa.

Reason

Cross Contamination with Other Products: Four lots of Liothyronine Sodium Tablets, USP 5 mcg are being recalled due to the finding of a potential carryover of trace amounts of a previously manufactured product.

Identifiers

ndc42794-018-02
ndc42794-018-12
ndc42794-018-06
ndc42794-019-02
ndc42794-019-06
ndc42794-019-12
ndc42794-020-02
ndc42794-020-12
code_infoLot #s: a) 1302201, Exp 01/2015; 1305501, Exp 03/2015; 1314801, Exp 10/2015; b) 1302202, Exp 01/2015

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-1344-2014%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.