Titanium 4000 recall
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
Why was Titanium 4000 recalled?
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
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?
Expiration 12/29/2020
- Product
- Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
- Recalling firm
- D.B.P. Distribution
- Quantity
- unknown
- Distribution
- Nationwide.
- Recall date
- May 22, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)