FDAClass IIAugust 14, 2019

Sperm Booster recall: CGMP Deviations

Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Why was Sperm Booster recalled?

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

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 within expiry

Product
Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Recalling firm
Herbal Doctor Remedies
Quantity
N/A
Distribution
Nationwide within the United States and Brazil and on the internet
Recall date
August 14, 2019
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls