FDA Food EnforcementOther / 其他

Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count Capsules. Product labeling reads in part:"MAX LUNG AID Extra Strength Dietary Supplement 100 CAPSULES0 65176 26289 8HealthMax Products Inc. Altadena, CA 91001". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES0 65176 30266 2Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001".

Recall F-1933-2013Published 2013-10-02Company Healthmaxx Global Inc.

Reason / 召回原因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.

Distribution / 销售地区CA, MD, and NY

Code information / 批次信息Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2

Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情：以原始机构公告为准

Recall number / 召回编号

F-1933-2013

Classification / 风险等级

Other / 其他

Published / 发布时间

2013-10-02

Recalling firm / 召回企业

Healthmaxx Global Inc.

Product description / 产品描述

Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count Capsules. Product labeling reads in part:"MAX LUNG AID Extra Strength Dietary Supplement 100 CAPSULES***0 65176 26289 8***HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES***0 65176 30266 2***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2

Product quantity / 产品数量

1,746 bottles

Distribution / 销售地区

CA, MD, and NY

Reason for recall / 召回原因

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.

Need the original notice?
Open the agency source for the complete official notice and any disposal, return, or contact instructions.

Open official source ↗

← Return to Recall Radar search / 返回搜索雷达

Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.