FDA Food recall F-1927-2013
Hyper II LECITHIN, 100 Count Softgels
- FDA Food
- Class III
- terminated
- Published 2013-10-02
On 2013-10-02 the FDA classified a Class III recall of Hyper II LECITHIN, 100 Count Softgels by Healthmaxx Global, citing 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 labe….
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1927-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-06-10 |
| Published | 2013-10-02 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Healthmaxx Global |
| Distribution | CA, MD, NY |
Product
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***".
Reason
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.
Identifiers
| upc | 665176011153 |
|---|---|
| code_info | Lot # LIN0130 UPC 6 65176 01115 3 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1927-2013%22
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