FDAClass IFebruary 22, 2017

SLIMFIT X capsules recall

SLIMFIT X capsules, packaged in a 60-cont bottle

Why was SLIMFIT X capsules recalled?

Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All lots and all expiration dates.

Product
SLIMFIT X capsules, packaged in a 60-cont bottle
Recalling firm
Jersey Shore Supplements, LLC
Quantity
150 bottles
Distribution
New Jersey and Maryland.
Recall date
February 22, 2017
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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