RecallRadar

FDA Drug recall D-528-2013

Lusair Liquid, 1 PINT bottle, OTC, Marketed by: Pernix Therapeutics, Gonzales, LA 70737 NDC 23359-017-16

On 2013-06-12 the FDA classified a Class II recall of Lusair Liquid, 1 PINT bottle, OTC, Marketed by: Pernix Therapeutics, Gonzales, LA 70737 NDC 23359-017-16 by Tg United, citing CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-528-2013
ClassificationClass II
Statusterminated
Initiated2013-01-30
Published2013-06-12
Last updated2026-09-13 11:51 UTC
CompanyTg United
DistributionFL, LA, MS, SC, TX

Product

Lusair Liquid, 1 PINT bottle, OTC, Marketed by: Pernix Therapeutics, Gonzales, LA 70737 NDC 23359-017-16

Reason

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Identifiers

code_info
Lot# 11AQ004 Exp. 12/12; Lot# 11AQ005 Exp. 12/12; Lot # 11AQ006 Exp. 12/12; Lot# 11AQ007 Exp. 12/12; Lot # 11BQ012 -…Lot# 11AQ004 Exp. 12/12; Lot# 11AQ005 Exp. 12/12; Lot # 11AQ006 Exp. 12/12; Lot# 11AQ007 Exp. 12/12; Lot # 11BQ012 - 19728 20 mL, Exp. 01/13; Lot# 11LQ003 Exp. 10/13; Lot# 11LQ004 Exp. 10/13; Lot# 11LQ005 Exp 10/13; Lot# 11LQ006 Exp. 10/13.

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-528-2013%22

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