Lower riskFood recall · FDA · Published April 27, 2021
PUBLIC GOODS Hair Skin Nails Supplement Recall: Undeclared Soy Risk
PUBLIC GOODS Hair, Skin & Nails dietary supplements with 60 tablets may contain undeclared soy. Consumers should check lot numbers 190063 or 19250: recall due to potential soy allergen.
“PUBLIC GOODS Hair Skin Nails Supplement Recall: Undeclared Soy Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14591-public-goods-hair-skin-nails-supplement-recall-undeclared-soy-risk. Based on FDA recall #F-0494-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0494-2021%22&limit=1).
The FDA announced on April 27, 2021, that PUBLIC GOODS voluntarily recalled its HAIR, SKIN, & NAILS Dietary Supplement due to undeclared soy. Owners should contact the company for a refund. The recall affects 3,733 bottles distributed nationwide.
How to tell if you have it
Brand: PUBLIC GOODS
Product: HAIR, SKIN, & NAILS Dietary Supplement
Size: 60 tablets per bottle
Lot codes: Lot#190063, Lot#192505
The hazard
The product may contain undeclared soy. The record lists fish gelatin from cod, pollack, haddock, hake, cusk, redfish, sole, and/or flounder as an allergen.
Context
GovInfoNow's records show other recent recalls of similar products include Stuffed Foods Cacio e Pepe Arancini Recall (2025-11-12), Ukrop's Cake Recall (2025-12-11), and Prospector Popcorn Recall (2026-04-28).
How to tell if you have this one
Check the product label for the brand 'PUBLIC GOODS' and the lot numbers 190063 or 192505. The product is a dietary supplement with 60 tablets per bottle.
Brand
PUBLIC GOODS
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot numbers 190063 or 192505 on the product label.
Where it went and when
Where it was distributed
Distributed in 50 states and D.C..
Listed by the agency
Not listed
FDA distribution: “AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 16 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-0494-2021 (April 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0494-2021 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.