FDA recall D-896-2013

Product

Duet DHA 400 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Rx only, Manufactured for Eckson Labs, Wilmington, DE (NDC 44118-809-30) and Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-809-30)

Reason for recall

Subpotent; Beta carotene (Vitamin A)

Distribution

Nationwide.

Key facts

Status

Terminated

Initiation date

2013-06-28

Report date

2013-08-28

Termination date

2014-05-27

Voluntary/Mandated

Voluntary: Firm initiated

Location

Suwanee, GA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-896-2013