CLASS II Food recall · Reported 13 Dec 2023 · FDA Enforcement Report

RM-10 Ultra, Ultimate Immune System Support60 Vegetarian recalled

Garden Of Life is recalling RM-10 Ultra, Ultimate Immune System Support60 Vegetarian Caplets, Whole Food Dietary. The recall was initiated on 19 Oct 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Numbers: 50304364, 50298662 Exp. Dates: 2/2024-9/2024
Quantity recalled8,940 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0484-2024
FDA event ID
93289
Recalling firm
Garden Of Life, West Palm Beach, FL
Brand
Garden
Classification
Class II
Status
Terminated
Recall initiated
19 Oct 2023
FDA classified
1 Dec 2023
Reported
13 Dec 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Soy
Product category
Dietary Supplements

Timeline

19 Oct 2023Recall initiated by company
1 Dec 2023Classified by FDA+43 days
13 Dec 2023Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Soy.

Product as listed by the FDA

Garden of Life, RM-10 ULTRA, Ultimate Immune System Support60 Vegetarian Caplets, Whole Food Dietary Supplement, 90 Ultra Zorbe Vegetarian Capsules

Where it was distributed

Domestic and foreign distribution.

Questions about this recall

Why was it recalled?

Undeclared Soy.

Which lots are affected?

Lot Numbers: 50304364, 50298662 Exp. Dates: 2/2024-9/2024

Where was it sold?

Domestic and foreign distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 93289

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