FDA recall D-894-2013

Product

Duet DHA Balanced, 1) 30 count tablet blister cards and 5 count softgels blister cards combination pack (NDC 44118-775-30 and NDC 44118-800-30) 2) physician samples (carton contain 7 envelopes each with one 5 count tablet blister card and 5 softgels (NDC 44118-800-05) Rx only, Manufactured for Eckson Labs, Wilmington, DE

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-894-2013