guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000850

Recall Number: D-684-2014

Firm: Aidapak Services, LLC

Classification: Class II

Status: Terminated

Report Date: 20140122

Initiation Date: 20130702

Termination Date: 20140207

Reason for Recall

Labeling:Label Mixup; guaiFENesin ER Tablet, 600 mg may be potentially mislabeled as OMEGA-3-ACID ETHYL ESTERS, Capsule, 1000 mg, NDC 00173078302, Pedigree: W003243, EXP: 6/17/2014.

Product Description

guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000850