CLASS I Drug recall · Reported 26 Oct 2016 · FDA Enforcement Report
Ginseng Power-X , 1800 mg per pack packs recalled by SOS Telecom
SOS Telecom is recalling Ginseng Power-X , 1800 mg per pack packs per, distributed in New York. The recall was initiated on 12 May 2016 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-0103-2017
- FDA event ID
- 74144
- Recalling firm
- SOS Telecom, Bayside, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 12 May 2016
- FDA classified
- 14 Oct 2016
- Reported
- 26 Oct 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 12 May 2016 | Recall initiated by company | |
| 14 Oct 2016 | Classified by FDA | +155 days |
| 26 Oct 2016 | 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 sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
Product as listed by the FDA
Ginseng Power-X , 1800 mg, 1 capsule per pack , 24 single packs per box.
Where it was distributed
NY
Questions about this recall
Is Ginseng Power-X , 1800 mg per pack packs per recalled?
Yes. SOS Telecom recalled Ginseng Power-X , 1800 mg per pack packs per on 12 May 2016. The recall is Class I and its status is Terminated. Recall number D-0103-2017.
Why was it recalled?
Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
Which lots are affected?
Lot: 7788965; Best use by: 10/15/2018
Where was it sold?
NY
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 SOS Telecom
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Ninja-X, 4200 mg per pack packs recalled by SOS Telecom | SOS Telecom | Labeling Errors | NY |
| Drug | CLASS I | Tiger-X, 1200 mg per pack packs recalled by SOS Telecom | SOS Telecom | Labeling Errors | NY |
| Drug | CLASS I | Super Samurai-X , 1000 mg per pack packs recalled by SOS Telecom | SOS Telecom | Labeling Errors | NY |