Healthmaxx Global Inc.: 28 FDA recall reports
Every food recall the FDA has published for Healthmaxx Global Inc.. The fault, and how the agency graded it.
28Reports
1Class I
0Ongoing
2013-10-02Most recent
1 Class I on this pageClass I means the FDA judged there was a reasonable probability of serious harm or death. Check the lot numbers against anything you hold.
What the classes mean
The FDA sorts every recall into one of three classes. The class is the whole story. It is also the part people skip.
Class II is the bulk of every list here. That matters. A long list of Class II says something different from one Class I.
By class
Checking whether it affects you
The lot or code number is what matters. Not the product name. A recall covers
specific lots. Yours may not be one of them.
Check the code on your package against the report. The FDA keeps the current
list at fda.gov/safety/recalls.
The reports
The text below is quoted from the FDA record word for word.
MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supple
F-1938-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6".
- Where it went
- CA, MD, and NY
- How much
- 2,659 bottles
Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Sup
F-1916-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads in part:"Manufactured for: HealthMax Products Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 7,074 bottles
MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII
F-1925-2013 · Class II · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII Dietary Supplement 100 Softgels*** 0 65176 08108 6***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 9069 bottles
MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance*
F-1934-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958 5***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 5,223 bottles
MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130
F-1931-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 7***HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 2,245 bottles
Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fis
F-1926-2013 · Class II · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% DHA - 30% EPA***Dietary Supplement 100 Softgels***6 65176 05274 3***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 2863 bottles
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count
F-1928-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG, 200 Count Softgels. Product labeling reads in part:"LIVERAID***Dietary Supplement 200 Softgels***6 65176 82031 1***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"LIVER AID***DIETARY SUPPLEMENT 200 Softgels***6 65176 02434***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG***Dietary Supplment 200 Softgels***0 65176 06068 5***Manufactured in FDA Approved GMP Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 5775 bottles
MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 C
F-1922-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 3197 bottles
MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg***DIETARY SUP
F-1940-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg***DIETARY SUPPLEMENT 300 Capsules***6 65176 25166 5***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 8,059 bottles
MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple S
F-1917-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 120 Tablets***6 65176 08218 4***Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 18,876 bottles
Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUP
F-1943-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Altadena, CA 91001
- Where it went
- CA, MD, and NY
- How much
- unknown
Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Cou
F-1921-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200 Count Softgels. Product labeling reads in part:"LIVERAID***Dietary Supplement 200 Softgels***6 65176 82031 1***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"LIVER AID***DIETARY SUPPLEMENT 200 Softgels***6 65176 02434 4***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG Dietary Supplement 200 Softgels***0 65176 06068***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 5775 bottles
MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Gluco
F-1919-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg***200 Tablets***6 65176 60566 6***Manufactured in FDA Approved facility for: HealthMax Products, Inc. Altadena, CA 91001***"
- Where it went
- CA, MD, and NY
- How much
- unknown
MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsul
F-1930-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 65176 30162 9***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 6,126 bottles
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Cou
F-1933-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- 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***".
- Where it went
- CA, MD, and NY
- How much
- 1,746 bottles
MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STREN
F-1937-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176 51257 3***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 3,816 bottles
MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PR
F-1924-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels***6 65176 31465 0***Manufactured For:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 2318 bottles
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVO
F-1939-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA PROBIOTICS, 90 Count Capsules Product labeling reads in part:"MAX SOY ISOFLAVONES MENOPAUSE SUPPORT**DIETARY SUPPLEMENT 90 CAPSULES***6 65176 53126 2***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX ULTRA PROBIOTICS***90 Capsules Dietary Supplement***6 65176 30625 9***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 6,379 bottles
Class I
MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 ***D
F-1923-2013 · Class I · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 ***Dietary Supplement 180 Tablet***0 65176 06756 1***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 4139 bottles
MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry***Die
F-1935-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry***Dietary Supplement 100 CAPSULES***6 65176 62165 9***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 5,124 bottles
MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Suppl
F-1932-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Supplement 200 Capsules***6 65176 32608 0***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 4,531 bottles
MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:"MAX KIDNEY STRONG***Dietary Supp
F1920-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:"MAX KIDNEY STRONG***Dietary Supplement 120 Tablets***6 65176 13427 2***Manufactured for: HealthMax Products, Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 1972 bottles
Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Suppleme
F-1927-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- 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***".
- Where it went
- CA, MD, and NY
- How much
- 817 bottles
Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMEN
F-1942-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 100 capsules***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***".UPC 0 65176 26289 8
- Where it went
- CA, MD, and NY
- How much
- unknown
MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic
F-1936-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic OPC31 Grapeseed Extract***NEW WITH BLUEBERRY***Dietary Supplement 200 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 4,022 bottles
Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 150
F-1941-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 150 tablets***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***".UPC 6 65176 52047 1
- Where it went
- CA, MD, and NY
- How much
- Unknown
MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple S
F-1918-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 300 Tablets***6 65176 36159 3***Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA 91001***".
- Where it went
- CA, MD, and NY
- How much
- 3,835 bottles
MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(
F-1929-2013 · Class III · reported 2013-10-02 · Terminated
- Why it was 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.
- Product
- MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***".
- Where it went
- CA, MD, and NY
- How much
- 31,259 bottles
Read these counts with three things in mind
A firm with more recalls usually makes more products. A contract packer runs
hundreds of lines. It will out-recall a company with one product whatever either
does. This is not a safety ranking.
Most recalls here are voluntary. A firm found its own fault and pulled the stock.
That is the system working. It lands in this database looking the same as a recall
the FDA had to push for.
Terminated means the FDA considers the recall finished. It is not a verdict.
It does not mean anyone was harmed.
Source: openFDA enforcement reports, retrieved 2026-08-05. FDA dataset last updated 2026-07-29.
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