Lower riskFood recall · FDA · Published May 4, 2021
Bloommy Biotin Collagen Keratin Capsules Recall: Undeclared Fish Collagen
Bloommy recalls biotin collagen keratin capsules for skin, joint and hair supplements due to undeclared fish collagen. Consumers should check product labels for the recall.
“Bloommy Biotin Collagen Keratin Capsules Recall: Undeclared Fish Collagen.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14560-bloommy-biotin-collagen-keratin-capsules-recall-undeclared-fish-collagen. Based on FDA recall #F-0542-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0542-2021%22&limit=1).
The FDA announced on May 4, 2021, that bloommy Inc. is recalling Bloomy Biotin Collagen Keratin Capsules because the dietary supplement contains undeclared fish collagen. The nationwide e-commerce recall affects 74,598 units and has been classified as Class II.
Manufacturer: bloommy Inc., 106 W. Broad St. Pawcatuck, CT 06379
Quantity: 74,598 units
The hazard
The product contains undeclared fish collagen, which poses an allergy risk to individuals with fish allergies. The FDA classified the recall as Class II.
Context
GovInfoNow's records show that Mellish Island issued a recall on July 1, 2026, for undeclared fish collagen in its Super Skin product. Other recent recalls of similar products include Organiccs Collagen (Sept. 14, 2026) and Koi Koi Trading Fish Balls (Jan. 28, 2026).
How to tell if you have this one
Check for the product name 'Bloomy*** Biotin Collagen Keratin Capsules for SKIN, JOINT, HAIR' on the label. The product was manufactured by Bloommy Inc. in Pawcatuck, CT.
Brand
Bloommy
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the product name 'Bloomy*** Biotin Collagen Keratin Capsules for SKIN, JOINT, HAIR' on the label.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide through e-commerce” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0542-2021 (May 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0542-2021 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.