CLASS III Food recall · Reported 2 Oct 2013 · FDA Enforcement Report

Hyper II Lecithin Softgels recalled by Healthmaxx Global

Healthmaxx Global is recalling Hyper II Lecithin Softgels, distributed in California, Maryland, New York. The recall was initiated on 10 Jun 2013 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot # LIN0130 UPC 6 65176 01115 3
Quantity recalled817 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1927-2013
FDA event ID
65733
Recalling firm
Healthmaxx Global, Hacienda Heights, CA
Classification
Class III
Status
Terminated
Recall initiated
10 Jun 2013
FDA classified
24 Sep 2013
Reported
2 Oct 2013
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors
Product category
Dietary Supplements

Timeline

10 Jun 2013Recall initiated by company
24 Sep 2013Classified by FDA+106 days
2 Oct 2013Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.

Product as listed by the FDA

Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".

Where it was distributed

CA, MD, and NY

CaliforniaMarylandNew York

Questions about this recall

Is Hyper II Lecithin Softgels recalled?

Yes. Healthmaxx Global recalled Hyper II Lecithin Softgels on 10 Jun 2013. The recall is Class III and its status is Terminated. Recall number F-1927-2013.

Why was it recalled?

In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.

Which lots are affected?

Lot # LIN0130 UPC 6 65176 01115 3

Where was it sold?

CA, MD, and NY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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