Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792
Summary
The FDA issued a Class II for Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distribu by Mellish Island Corp. Reason: Firm's finished product label does not declare the source of marine collagen which was determined to be fish..
Details
Source
Food Recall
External ID
H-1190-2026
Action Date
2026-08-05
Status
Ongoing
Category
food
Product Description
Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3
Lot/Code Info: Lot: CA1G24 Expiration: 08-2027
Quantity Affected: 1,600 bottles
Reason for Recall
Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
Distribution
Product is distributed through TikTok exclusively. Presumably nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-01
Company
San Dimas, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 14 food recalls issued in the same week, part of 53 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mellish Island Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mellish Island Corp have FDA actions?
This is the only FDA action we have on record for Mellish Island Corp in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1190-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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