CLASS I Drug recall · Reported 20 Sep 2017 · FDA Enforcement Report
Super Panther 7K Capsules 1250 mg blend, a) blister cards recalled
Chiavna Saffron is recalling Super Panther 7K Capsules 1250 mg blend, a) blister cards, distributed nationwide in the US. The recall was initiated on 21 Jul 2017 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-1145-2017
- FDA event ID
- 77812
- Recalling firm
- Chiavna Saffron, Huntersville, NC
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Jul 2017
- FDA classified
- 12 Sep 2017
- Reported
- 20 Sep 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 21 Jul 2017 | Recall initiated by company | |
| 12 Sep 2017 | Classified by FDA | +53 days |
| 20 Sep 2017 | Published in enforcement report | +8 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 be tainted with sildendafil and tadalafil
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Super Panther 7K Capsules 1250 mg blend, a) 1 count blister cards shipped in boxes of 30 (UPC# 6015577513247); and b) 6 count bottles (UPC# 601577513209), Distributed by SX Power CO., Brooklyn, NY
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA;FDA analysis found product to be tainted with sildendafil and tadalafil
Which lots are affected?
a) RO846356 Exp. 8/28/2020; b) RO246852 Exp. 8/28/2020
Where was it sold?
Nationwide
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.