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Lower risk Food recall · FDA · Published May 25, 2021

Naturo Aid Vita Aid SynerClear (Unflavoured) Powder Recall: Undeclared Milk Risk

Naturo Aid recalls Vita Aid SynerClear (Unflavoured) powder (VA-925) due to potential milk contamination. Products may contain undeclared milk residue. Check lot numbers 136077P1 (exp 12/2023) or 144876P1A (exp 03/2023).

🇺🇸 FDA recall #F-0978-2021FoodNaturo Aid ›
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Recalling firmNaturo Aid Pharmaceutical Inc.20285 Stewart Cres Unit 302 · Maple Ridge, Canada
✎ GovInfoNow plain-language explainer

What happened, in plain English

Naturo Aid is recalling Vita Aid SynerClear (Unflavoured) powder (VA-925) because it may contain undeclared milk residue. This could pose a risk for people with milk allergies or sensitivities. The recall affects specific lot numbers with expiration dates. Read more at govinfonow.com/recall/14475-naturo-aid-vita-aid-synerclear-unflavoured-powder-recall-undeclared-milk.

Source Summary by GovInfoNow · govinfonow.com/recall/14475-naturo-aid-vita-aid-synerclear-unflavoured-powder-recall-undeclared-milk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0978-2021

Cite this page

“Naturo Aid Vita Aid SynerClear (Unflavoured) Powder Recall: Undeclared Milk Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14475-naturo-aid-vita-aid-synerclear-unflavoured-powder-recall-undeclared-milk. Based on FDA recall #F-0978-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0978-2021%22&limit=1).

Why it’s dangerous

The product may contain undeclared milk residue due to contamination during manufacturing. This could cause allergic reactions in individuals sensitive to milk, including hives, swelling, or more severe reactions in rare cases.

Who’s affected

People who have purchased Vita Aid SynerClear (Unflavoured) powder (VA-925) with lot numbers 136077P1 (expiring 12/2023) or 144876P1A (expiring 03/2023) are affected. Those with milk allergies or sensitivities are at higher risk.

How to tell if you have this one

Check the product label for lot numbers 136077P1 (expiring December 2023) or 144876P1A (expiring March 2023). The product is a 650g powder in a plastic bottle with a white cap.

  • Brand
    Naturo Aid
  • Category
    Food
FDA recall event · 5 products

All 5 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
    Distributed in Arizona, California, Florida, Kansas, Minnesota, Montana, New Jersey, Oregon, Pennsylvania, and Washington.
Recall numberProduct, codes & lotsQuantity
F-0976-2021Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a net weight of 315g.; Lot 165576P1A (expiry date 03/2022); Lot 165876P1 (expiry date 05/2022)910 units
F-0977-2021Vita Aid Keto-Elemental Nutrition (Thai), VA-958. The product is a powder, packaged in an aluminum bag , with a net weight of 315g.; Lot 173876P1 (expiry date 04/2022); Lot 173876P1A (expiry date 04/2022).268 units
F-0978-2021Vita Aid SynerClear (Unflavoured), VA-925. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.; Lot 136077P1 (expiry date 12/2023); Lot 144876P1A (expiry date 03/2023).302 units
F-0979-2021Vita Aid SynerClear (Vanilla), VA-924. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.; Lot 136177P1 (expiry date 12/2023); Lot 144876P2 (expiry date 03/2023).3072 units
F-0980-2021Vita Aid SynerClear (Chocolate), VA-012. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.; Lot 136377P1 (expiry date 12/2023) and Lot 163776P1 (expiry date 03/2023).1026 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers 136077P1 (expiring 12/2023) or 144876P1A (expiring 03/2023) on the product label.

Where it went and when

Where it was distributed

Distributed in 10 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: yesMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Distributed in Arizona, California, Florida, Kansas, Minnesota, Montana, New Jersey, Oregon, Pennsylvania, and Washington.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Florida, Kansas, Minnesota, Montana, New Jersey, Oregon, Pennsylvania, Washington.

Recall timeline

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

1. Firm started the recall: May 25, 202112. FDA classified it Class II: Sep 13, 202123. FDA terminated the recall: Sep 21, 202134. Published in FDA’s Enforcement Report: Sep 22, 202142021
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-0978-2021 (May 25, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0978-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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