Actra-SX 500 Capsules recall
Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
Why was Actra-SX 500 Capsules recalled?
Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction
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 number 008A, expiration date Dec 2014, UPC code 830733002016
- Product
- Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
- Recalling firm
- Body Basics Inc
- Quantity
- 30,000 capsules
- Distribution
- Nationwide
- Recall date
- April 24, 2013
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)