Poseidon Platinum 3500 capsule recall
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Why was Poseidon Platinum 3500 capsule recalled?
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared sildenafil and tadalafil making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.
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 distributed 07/01/2019 through 09/28/2020.
- Product
- Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
- Recalling firm
- Yamtun7
- Quantity
- 36 capsules
- Distribution
- Unknown; unable to determine due to firm's Ebay account being closed.
- Recall date
- July 21, 2021
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)