Skip to content
Stop using now Food recall · FDA · Published June 4, 2021

Bomunity Paximune Recall: Bacterial Contamination Risk

Bomunity Ltd Co recalls Paximune Dietary Supplement due to potential bacterial contamination. Check lot 210402 and UPC 64395 00001.

🇺🇸 FDA recall #F-0817-2021FoodBomunity ›
Take action

Contact the company

Recalling firmBomunity Ltd Co13351 E Fm 1151 · Amarillo, TX 79118-5616
✎ GovInfoNow plain-language explainer

Bomunity Ltd Co is recalling Paximune Dietary Supplement, a bovine protein supplement packaged in dark glass bottles. The product may be contaminated with bacteria, posing a health risk to consumers. This recall affects 3,540 cases distributed nationwide throughout the US. Read more at govinfonow.com/recall/14414-bomunity-paximune-recall-bacterial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/14414-bomunity-paximune-recall-bacterial-contamination-risk · Updated October 10, 2026 · FDA enforcement record: FDA #F-0817-2021

Cite this page

“Bomunity Paximune Recall: Bacterial Contamination Risk.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14414-bomunity-paximune-recall-bacterial-contamination-risk. Based on FDA recall #F-0817-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0817-2021%22&limit=1).

Bomunity Ltd Co recalled Paximune Dietary Supplement nationwide due to potential bacterial contamination, according to a June 4, 2021 Food and Drug Administration announcement.

How to tell if you have it

  • Brand: Bomunity
  • Product: Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz.
  • UPC: 6439500001
  • Lot: 210402

The hazard

The product may be contaminated with bacteria, the FDA said in its recall record.

Context

GovInfoNow's records show other recent recalls of similar products include Wellnov Joint Nourish Liquid Recall (2026-04-23), Wellnov FulviLife Complex Recall (2026-04-23) and Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops Recall (2026-04-23).

How to tell if you have this one

Look for Paximune Dietary Supplement in dark glass bottles containing 2 Fl. Oz. (60ml). Check the label for UPC 64395 00001 and LOT number 210402. The product was sold nationwide throughout the US.

  • Brand
    Bomunity
  • Product
    Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop using the supplement

    Do not consume Paximune Dietary Supplement due to the potential for bacterial contamination.

  2. Check your product details

    Verify if you have the recalled item by checking for UPC 64395 00001 and LOT 210402 on the dark glass bottle.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide throughout the US” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Jun 4, 202112. FDA classified it Class II: Aug 3, 202123. Published in FDA’s Enforcement Report: Aug 11, 202134. FDA terminated the recall: Sep 23, 202142021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0817-2021 (June 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0817-2021 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA