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Unrated Food recall · FDA · Published May 15, 2019

APS BioGroup Immulox Immune Balance Supplement Recall: Elevated APC Levels

APS BioGroup recalls Immulox Immune Balance Polypeptide Supplement due to elevated APC levels from Stenotrophomonas maltophilia. Consumers should check product details and contact for guidance.

🇺🇸 FDA recall #F-1481-2019FoodAPS BioGroup ›
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Contact the company

Recalling firmAPS BioGroup, Inc2235 S Central Ave · Phoenix, AZ 85004-2909
✎ GovInfoNow plain-language explainer

APS BioGroup is recalling Immulox Immune Balance Polypeptide Supplements because testing found elevated APC levels caused by Stenotrophomonas maltophilia bacteria. This could lead to health issues for people using the supplement. Read more at govinfonow.com/recall/17482-aps-biogroup-immulox-immune-balance-supplement-recall-elevated-apc-levels.

Source Summary by GovInfoNow · govinfonow.com/recall/17482-aps-biogroup-immulox-immune-balance-supplement-recall-elevated-apc-levels · Updated October 5, 2026 · FDA enforcement record: FDA #F-1481-2019

Cite this page

“APS BioGroup Immulox Immune Balance Supplement Recall: Elevated APC Levels.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17482-aps-biogroup-immulox-immune-balance-supplement-recall-elevated-apc-levels. Based on FDA recall #F-1481-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1481-2019%22&limit=1).

The FDA announced on May 15, 2019, that APS BioGroup, Inc. voluntarily recalled Immulox immune balance polypeptide supplements due to elevated levels of Stenotrophomonas maltophilia. The recall affects 7,132 units distributed nationwide and in Switzerland.

How to tell if you have it

  • Brand: APS BioGroup
  • Product: Immulox, UPC 1 82863 000064 6. Immune Balance Polypeptide Supplement with Naturally Occuring Bioactive Peptides. 5.07 oz (150 ml)
  • UPC: 01828630000646
  • Lot codes: 9068-2, 9068-3, 9068-4, 9068-5, 9068-6
  • Item numbers: #4044, #4691, #4181, #00064
  • Bulk numbers: UL-7
  • Expiration dates: 04/2021
  • Manufacturing date: April 21, 2019

The hazard

The FDA said the recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.

Context

GovInfoNow's records show other recent recalls of similar products include Aonic Complete His (2026-01-15) and Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops (2026-04-23). Ambriola Locatelli Grated Pec was also recalled on 2025-11-21 for Listeria Monocytogenes risk.

How to tell if you have this one

Check for the UPC 1 82863 000064 6 on the product label. The product was manufactured on April 21, 2019, and expires April 2021.

  • Brand
    APS BioGroup
  • Product
    Immulox, UPC 1 82863 000064 6. Immune Balance Polypeptide Supplement with Naturally Occuring Bioactive Peptides. 5.07
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide and Switzerland. No military/govt/VA consignees.
Recall numberProduct, codes & lots
F-1478-2019Immuno PRP Spray, UPC 8 12527 01176 2. Colostrum Polypeptides. 5 fl oz (140 mL); Manufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021
F-1479-2019Viralox, UPC 8 63784 00015 0. Immune Balancing Ploypeptide Oral Spray. 5.0 fl. oz. (150 ml) Oral Spray.; Manufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021
F-1480-2019DPS Throat Spray, UPC 8 55602 00021 3. Colostrum Immune Concentrate. Net 150 ml; Manufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021
F-1481-2019Immulox, UPC 1 82863 000064 6. Immune Balance Polypeptide Supplement with Naturally Occuring Bioactive Peptides. 5.07 oz (150 ml); Manufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 1 82863 000064 6 on the Immulox Immune Balance Polypeptide Supplement label.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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 and Switzerland. No military/govt/VA consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: May 15, 201912. FDA classified it Class II: Jun 18, 201923. Published in FDA’s Enforcement Report: Jun 26, 201934. FDA terminated the recall: Dec 27, 201942019
  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.

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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-1481-2019 (May 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1481-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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