CLASS I Drug recall · Reported 15 Jun 2016 · FDA Enforcement Report

Thin and Slim Extreme Stack Fat Burner Dietary Supplement recalled

Novacare is recalling Thin and Slim Extreme Stack Fat Burner Dietary Supplement, distributed nationwide in the US. The recall was initiated on 24 Aug 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 637687019133
Quantity recalledN/A

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-0969-2016
FDA event ID
71989
Recalling firm
Novacare, Murray, UT
Classification
Class I
Status
Terminated
Recall initiated
24 Aug 2015
FDA classified
6 Jun 2016
Reported
15 Jun 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

24 Aug 2015Recall initiated by company
6 Jun 2016Classified by FDA+287 days
15 Jun 2016Published in enforcement report+9 days

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

Reason for recall

Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of Salicylic acid in dietary supplements.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged in 90 capsule containers. TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Thin and Slim Extreme Stack Fat Burner Dietary Supplement recalled?

Yes. Novacare recalled Thin and Slim Extreme Stack Fat Burner Dietary Supplement on 24 Aug 2015. The recall is Class I and its status is Terminated. Recall number D-0969-2016.

Why was it recalled?

Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of Salicylic acid in dietary supplements.

Which lots are affected?

UPC 637687019133

Where was it sold?

Nationwide

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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