FDA Drug recall D-0101-2017
Tiger-X, 1200 mg, 1 capsule per pack , 24 single packs per box
- FDA Drug
- Class I
- terminated
- Published 2016-10-26
On 2016-10-26 the FDA classified a Class I recall of Tiger-X, 1200 mg, 1 capsule per pack , 24 single packs per box by Sos Telecom, citing 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.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0101-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-05-12 |
| Published | 2016-10-26 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Sos Telecom |
| Distribution | NY |
Product
Tiger-X, 1200 mg, 1 capsule per pack , 24 single packs per box
Reason
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
Identifiers
| code_info | Lot No: 9236999; Best use by: 12/16/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0101-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.