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Use caution Food recall · FDA · Published July 1, 2026

Mellish Island Super Skin Recall: Undeclared Fish Collagen

Mellish Island Corp recalls Super Skin dietary supplements because the label fails to declare fish as the source of marine collagen.

🇺🇸 FDA recall #H-1190-2026FoodMellish Island ›
✎ GovInfoNow plain-language explainer

Mellish Island Corp is recalling Super Skin, a dietary supplement sold in 60-capsule bottles. The recall is necessary because the product label does not declare that the marine collagen ingredient is derived from fish. This omission poses a risk to consumers with fish allergies who rely on ingredient labels for safety. Read more at govinfonow.com/recall/157979-mellish-island-super-skin-recall-undeclared-fish-collagen.

Source Summary by GovInfoNow · govinfonow.com/recall/157979-mellish-island-super-skin-recall-undeclared-fish-collagen · Updated October 9, 2026 · Official notice: FDA #H-1190-2026

Cite this page

“Mellish Island Super Skin Recall: Undeclared Fish Collagen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/157979-mellish-island-super-skin-recall-undeclared-fish-collagen. Based on FDA recall #H-1190-2026.

The FDA announced on July 1, 2026, that Mellish Island Corp is recalling its Super Skin dietary supplement because the label fails to declare the source of marine collagen as fish. The recall affects 1,600 bottles distributed exclusively through TikTok.

How to tell if you have it

  • Mellish Island Super Skin Dietary Supplement
  • 60 Capsules, 2 per day
  • UPC: 8 58792 00332 3
  • Lot: CA1G24
  • Expiration: 08-2027

The hazard

The firm's finished product label does not declare the source of marine collagen, which was determined to be fish. This omission creates a potential allergen risk for consumers with fish allergies.

Context

GovInfoNow's records show other recent recalls of similar products include Pack'n Fresh Hondashi Seasoning Recall (2026-07-09), TG Foods Divided Sunset Collagen Peptides Recall (2026-02-27), and Gellert Global Group Kimbap Recall (2026-06-25).

How to tell if you have this one

Check your bottles for the brand name 'Mellish Island Super Skin', a UPC of 8 58792 00332 3, and Lot number CA1G24. The product is distributed exclusively through TikTok and has an expiration date of 08-2027.

  • Brand
    Mellish Island
  • Product
    Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product details

    Verify if you have the recalled bottles by checking the UPC (8 58792 00332 3) and Lot number (CA1G24).

  2. Avoid consumption if allergic

    If you have a fish allergy, do not consume the product as the label does not warn of this ingredient.

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: “Product is distributed through TikTok exclusively. Presumably nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 35 days after the firm started it.

1. Firm started the recall: Jul 1, 202612. FDA classified it Class II: Jul 28, 202623. Published in FDA’s Enforcement Report: Aug 5, 202634. Added to GovInfoNow: Aug 11, 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-1190-2026 (July 1, 2026)
  • 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