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Stop using now Food recall · FDA · Published September 14, 2026

Organiccs Collagen Recall: Undeclared Crab Shell Allergen

Pacific Health Sciences recalls Organiccs Absolutely Pure Collagen Peptides due to undeclared crab shell. Check your bottle if you have allergies.

🇺🇸 FDA recall #H-1401-2026FoodOrganiccs ›
✎ GovInfoNow plain-language explainer

What happened, in plain English

Pacific Health Sciences Llc is recalling Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides because the product contains undeclared crab shell. This ingredient was part of the glucosamine sulfate source and poses a risk to individuals with shellfish allergies. The recall affects approximately 395 units distributed to medical offices in several states. Read more at govinfonow.com/recall/1434252-pacific-health-sciences-llc-recalls-organiccs-absolutely-pure-type-1.

Source Summary by GovInfoNow · govinfonow.com/recall/1434252-pacific-health-sciences-llc-recalls-organiccs-absolutely-pure-type-1 · Published October 13, 2026 · Updated October 13, 2026 · Official notice: FDA #H-1401-2026

Cite this page

“Organiccs Collagen Recall: Undeclared Crab Shell Allergen.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/1434252-pacific-health-sciences-llc-recalls-organiccs-absolutely-pure-type-1. Based on FDA recall #H-1401-2026.

Why it’s dangerous

The presence of undeclared crab shell means that people with shellfish allergies could inadvertently consume the allergen. This can trigger a serious allergic response, ranging from hives to anaphylaxis, without their knowledge.

Who’s affected

Consumers who purchased this supplement, particularly those with known shellfish or crab allergies, are at risk of an allergic reaction. The product was primarily distributed to private practice medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii.

How to tell if you have this one

Look for Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides in 180 Veggie Capsules bottles. The specific lot number is 25009CP. The product was sold through private practice medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii.

  • Brand
    Organiccs
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Organiccs Absolutely Pure Collagen Peptides if you have a shellfish allergy or if your bottle matches the recalled lot number.

  2. Check your bottle details

    Verify that your product is the 180 Veggie Capsules version with lot number 25009CP.

  3. Contact the medical office

    Since distribution was primarily to private practice medical offices, contact the specific office where you obtained the supplement for further instructions.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product is primarily distributed to private practice medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Hawaii, Kentucky, Massachusetts, Oregon, Washington.

Recall timeline

FDA published this recall 23 days after the firm started it.

1. Firm started the recall: Sep 14, 202612. FDA classified it Class II: Sep 29, 202623. Published in FDA’s Enforcement Report: Oct 7, 202634. Added to GovInfoNow: Oct 13, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

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 #H-1401-2026 (September 14, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 13, 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