CLASS I Drug recall · Reported 22 Jan 2020 · FDA Enforcement Report
Panther Platinum, in green, black background with white recalled
Motto International is recalling Panther Platinum, in green, black background with white, red text in hologram paper, distributed in Texas. The recall was initiated on 17 Dec 2019 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0657-2020
- FDA event ID
- 84526
- Recalling firm
- Motto International, Dallas, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 17 Dec 2019
- FDA classified
- 10 Jan 2020
- Reported
- 22 Jan 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Packaging Defects
Timeline
| 17 Dec 2019 | Recall initiated by company | |
| 10 Jan 2020 | Classified by FDA | +24 days |
| 22 Jan 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Panther Platinum 30000 Capsules, in green, black background with white, red text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
Where it was distributed
TX
Questions about this recall
Is Panther Platinum, in green, black background with white, red text in hologram paper recalled?
Yes. Motto International recalled Panther Platinum, in green, black background with white, red text in hologram paper on 17 Dec 2019. The recall is Class I and its status is Terminated. Recall number D-0657-2020.
Why was it recalled?
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
Which lots are affected?
All lots remaining within expiry.
Where was it sold?
TX
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Motto International
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Stallion Platinum in blue,orange,white background recalled | Motto International | Packaging Defects | TX |
| Drug | CLASS I | Rhino 7 Platinum, in blue,orange,black background recalled | Motto International | Packaging Defects | TX |
| Drug | CLASS I | Bull Platinum, 1000 mg, in orange, white recalled by Motto International | Motto International | Packaging Defects | TX |