Antoto-K: Drug Recall
Recall #D-0366-2021 · 03/26/2021
Class II: Risk
Recall Details
- Recall Number
- D-0366-2021
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Antoto-K
- Status
- Terminated
- Date Initiated
- 03/26/2021
- Location
- Manassas, VA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 200 cartons
Reason for Recall
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of sildenafil and tadalafil.
Product Description
Thumbs Up 7 Red 70K, 10 count blister pack cartons, Distributed by Ummzy LLC., Made in USA, UPC 6 17135 89467 3.
Distribution Pattern
Nationwide
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.