CLASS I Drug recall · Reported 12 Aug 2020 · FDA Enforcement Report

A Clean Choice CBD, Hemp Oil Extract Tincture recalled

Michigan Herbal Remedies is recalling A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg, distributed nationwide in the US. The recall was initiated on 18 Jun 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesFG003106
Quantity recalled350 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1454-2020
FDA event ID
85854
Recalling firm
Michigan Herbal Remedies, Jenison, MI
Classification
Class I
Status
Completed
Recall initiated
18 Jun 2020
FDA classified
4 Aug 2020
Reported
12 Aug 2020
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Labeling Errors

Timeline

18 Jun 2020Recall initiated by company
4 Aug 2020Classified by FDA+47 days
12 Aug 2020Published in enforcement report+8 days

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

Reason for recall

Chemical contamination: product contains elevated levels of undeclared lead.

Product as listed by the FDA

A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Road Suite 1, Saginaw, MI 48603

Where it was distributed

Nationwide via internet sales,retailers and distributors in the USA

Nationwide

Stores named: Online Retailers

Questions about this recall

Is A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg recalled?

Yes. Michigan Herbal Remedies recalled A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg on 18 Jun 2020. The recall is Class I and its status is Completed. Recall number D-1454-2020.

Why was it recalled?

Chemical contamination: product contains elevated levels of undeclared lead.

Which lots are affected?

FG003106

Where was it sold?

Nationwide via internet sales,retailers and distributors in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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