Check the Batch
Class IIITerminated in FDA datasetAug 16, 2013

LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription

Recalling firm: Atlantic Pro Nutrients, Inc. dba XYMOGEN

Why it was recalled

Product was labeled as a medical food as opposed to a dietary supplement.

Check your package

Compare the exact product and package details with the label you have.

ProductLipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription Distributed by: PharmaceutiX Orlando, Florida

FDA code information

UPC # N3 53731-001-06 9 Lot # 50001784 exp. 09/2014, lot # 50001783 exp. 09/2014, lot # 50002588 exp 11/2015, and lot # 50002587 exp. 11/2015

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription Distributed by: PharmaceutiX Orlando, Florida

Extracted codes and context

TypeCode / valueContext
lot50001783UPC # N3 53731-001-06 9 Lot # 50001784 exp. 09/2014, lot # 50001783 exp. 09/2014, lot # 50002588 exp 11/2015, and lot # 50002587 exp. 11/2015
lot50001784UPC # N3 53731-001-06 9 Lot # 50001784 exp. 09/2014, lot # 50001783 exp. 09/2014, lot # 50002588 exp 11/2015, and lot # 50002587 exp. 11/2015
lot50002587xp. 09/2014, lot # 50001783 exp. 09/2014, lot # 50002588 exp 11/2015, and lot # 50002587 exp. 11/2015
lot5000258853731-001-06 9 Lot # 50001784 exp. 09/2014, lot # 50001783 exp. 09/2014, lot # 50002588 exp 11/2015, and lot # 50002587 exp. 11/2015

Recall details

Recall number
F-0816-2014
Event ID
66135
FDA status
Terminated
Initiated
Aug 16, 2013
Reported
Jan 8, 2014
Classified
Dec 30, 2013
Terminated
May 2, 2014
Quantity
25,852 bottles (All Brands)
Location
Orlando, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Nationwide and Alaska Canada and China

FDA source record · F-0816-2014

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.