CLASS III Food recall · Reported 2 Jul 2025 · FDA Enforcement Report

Probese Caps, dietary supplement with Iron recalled by Preventics

Preventics is recalling Probese Caps, dietary supplement with Iron, distributed nationwide in the US. The recall was initiated on 30 Apr 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codes21874-19; 21874-20; 21874-21; 21874-22; 21874-23; 21874-24; 21874-25
Quantity recalled112,506 pills

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
H-0094-2025
FDA event ID
96839
Recalling firm
Preventics, Scottsdale, AZ
Classification
Class III
Status
Terminated
Recall initiated
30 Apr 2025
FDA classified
25 Jun 2025
Reported
2 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Dietary Supplements

Timeline

30 Apr 2025Recall initiated by company
25 Jun 2025Classified by FDA+56 days
2 Jul 2025Published in enforcement report+7 days

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

Reason for recall

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)

Where it was distributed

Distributed Nationwide in the United States.

Nationwide

Questions about this recall

Is Probese Caps, dietary supplement with Iron recalled?

Yes. Preventics recalled Probese Caps, dietary supplement with Iron on 30 Apr 2025. The recall is Class III and its status is Terminated. Recall number H-0094-2025.

Why was it recalled?

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Which lots are affected?

21874-19; 21874-20; 21874-21; 21874-22; 21874-23; 21874-24; 21874-25

Where was it sold?

Distributed Nationwide in the United States.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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