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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90908

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 16, 2022
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Seeking Health LLC

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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.

F-0048-2023
Recall number
F-0048-2023
Initiated
September 16, 2022
Classification
Class II
Status
Terminated
Recalling firm
Seeking Health LLC
Quantity
4021 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product label claim for copper is 0.5mg, but third-party lab results revealed product contains higher levels of copper.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

"LOT # 022221182, MFG 09/2021" and "LOT # 031022127, MFG 10/2021" Case Labels read in part: " LOT #: 022221182" and "LOT #: 031022127"

Distribution pattern

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.