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Unrated Drug recall · FDA · Published May 11, 2016

The Aloe Source Recalls Aloe Sport Liniment Due to CGMP Deviations

The Aloe Source is recalling Aloe Sport Liniment and Aloe Vera Liniment due to Current Good Manufacturing Practice (CGMP) deviations. Check your lot numbers.

🇺🇸 FDA recall #D-1053-2016DrugThe Aloe Source ›
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Recalling firmThe Aloe Source3101 Technology Dr Ste 135 · Plano, TX 75074-3728
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Aloe Source has recalled specific lots of Aloe Sport Liniment and Aloe Vera Liniment because they did not meet Current Good Manufacturing Practice (CGMP) standards. The recall covers products sold nationwide, including 8 fl oz tubes and bottles, as well as 1 fl oz plastic bottles. The record does not specify what the CGMP deviations were or if there is a known health risk to consumers. Read more at govinfonow.com/recall/42765-the-aloe-source-recalls-aloe-sport-liniment-due-to-cgmp.

Source Summary by GovInfoNow · govinfonow.com/recall/42765-the-aloe-source-recalls-aloe-sport-liniment-due-to-cgmp · Updated October 9, 2026 · FDA enforcement record: FDA #D-1053-2016

Cite this page

“The Aloe Source Recalls Aloe Sport Liniment Due to CGMP Deviations.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42765-the-aloe-source-recalls-aloe-sport-liniment-due-to-cgmp. Based on FDA recall #D-1053-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1053-2016%22&limit=1).

Why it’s dangerous

The recall is due to deviations from Current Good Manufacturing Practice (CGMP) standards. The record does not describe the specific nature of these deviations or explain how they might affect product safety, efficacy, or contamination levels.

Who’s affected

Consumers who purchased Aloe Sport Liniment or Aloe Vera Liniment from nationwide retailers between the manufacturing date and May 11, 2016. Individuals using these topical analgesics for pain relief are the primary group affected.

How to tell if you have this one

Check your product for the following details: Brand 'The Aloe Source' or 'Aloe Vera'; Product names 'Aloe Sport Liniment', 'Aloe Vera Liniment', or 'Sport Thermogenic Eucalyptus Cream'; Sizes 8 fl oz (tube or bottle) or 1 fl oz (plastic bottle); Lot number 1407012; Expiration date 03/17; NDC 58826-704-08; UPC 732295704089.

  • Brand
    The Aloe Source
  • Product
    aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube, ALOE VERA Liniment Topical Analgesic 8 fl oz. bottle, Manufactured
  • Category
    Drug

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: May 11, 201612. FDA classified it Class II: Jun 26, 201623. Published in FDA’s Enforcement Report: Jul 6, 201634. FDA terminated the recall: Mar 31, 2017420162017
  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 #D-1053-2016 (May 11, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1053-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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