CLASS I Drug recall · Reported 20 Sep 2017 · FDA Enforcement Report
New Kopi Jantan Tradisional Natural Herbs Coffee recalled
Bestherbs Coffee is recalling New Kopi Jantan Tradisional Natural Herbs Coffee, distributed nationwide in the US. The recall was initiated on 17 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-1144-2017
- FDA event ID
- 77768
- Recalling firm
- Bestherbs Coffee, Arlington, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 17 Jul 2017
- FDA classified
- 12 Sep 2017
- Reported
- 20 Sep 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Milk
Timeline
| 17 Jul 2017 | Recall initiated by company | |
| 12 Sep 2017 | Classified by FDA | +57 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: presence of undeclared desmethyl carbodenafil and undeclared milk.
Product as listed by the FDA
New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets, Made in Malaysia, USA Distributor: Bestherbscoffee LLC (USA), Email: [email protected]
Where it was distributed
Recalling firm only distributed to 2 consignees in TX; however recalling firm reported that product is then distributed U.S. nationwide to consumers via individuals or internet
Questions about this recall
Why was it recalled?
Marketed without an approved NDA/ANDA: presence of undeclared desmethyl carbodenafil and undeclared milk.
Which lots are affected?
UPC 557205060083 ,Exp 5/24/18
Where was it sold?
Recalling firm only distributed to 2 consignees in TX; however recalling firm reported that product is then distributed U.S. nationwide to consumers via individuals or internet
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.