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FDA source record Class II Terminated

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 8100...

Recall Date: 2022-09-16 Recalling Firm: Seeking Health LLC Record Ref: F-0048-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 8100... and names Seeking Health LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Seeking Health LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2022-09-16
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Product Description & Identification

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily. Servings per Container: 30. Copper (as copper gluconate) 0.5 mg 56%. Manufactured for and Distributed by: Seeking Health, LLC 3140 Mercer Ave. Bellingham, WA 98225 (800) 547-9812. Case labels read in part: Seeking Health LLC. Item #: OPMULTI-60-TAB, Optimal Multivitamin Chewable Case.

Reason for Recall / Hazard Identified

The product label claim for copper is 0.5mg, but third-party lab results revealed product contains higher levels of copper.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
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  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed in AL, AK, AZ, AR, CA, CO, CT, DE,GA, FL,HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MT, MN, MO, MS, , NC, ND, NE, NH, NJ, NM, NY,NV, OR, OH, OK, PA, TN, WI, TX, RI, SC, SD, UT, VA, VT, WY, WV, Washington DC, and WA states; as well as the countries of Australia, Bermuda, Canada, Hong Kong, Iceland, Japan, Netherlands, Norway, Serbia, Singapore, Sweden, United Kingdom.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0048-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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