FDAClass IAugust 7, 2013

Night Bullet Capsules recall

Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA

Why was Night Bullet Capsules recalled?

Marketed Without an Approved NDA/ANDA; product contains analogues of sildenafil and tadalafil which are active pharmaceutical ingredients in FDA-approved drugs used to treat erectile dysfunction (ED) making this product an unapproved new drug.

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?

Lot# B43N032, Exp 10/15

Product
Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
Recalling firm
Green Planet Inc
Quantity
429,619 capsules
Distribution
Nationwide.
Recall date
August 7, 2013
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls