CLASS I Drug recall · Reported 4 Dec 2013 · FDA Enforcement Report
J.R. Jack Rabbit All Natural Herbal Supplement recalled
Jack Rabbit is recalling J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24- per, Order at, distributed nationwide in the US. The recall was initiated on 12 Aug 2013 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-021-2014
- FDA event ID
- 65895
- Recalling firm
- Jack Rabbit, Melbourne, FL
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 12 Aug 2013
- FDA classified
- 27 Nov 2013
- Reported
- 4 Dec 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
Timeline
| 12 Aug 2013 | Recall initiated by company | |
| 27 Nov 2013 | Classified by FDA | +107 days |
| 4 Dec 2013 | Published in enforcement report | +7 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: Laboratory analysis conducted by the FDA has determined that J.R. Jack Rabbit Male Enhancement product was found to contain two undeclared active pharmaceutical ingredients: sildenafil and tadalafil.
Product as listed by the FDA
J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934
Where it was distributed
Nationwide
Questions about this recall
Is J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24- per, Order at recalled?
Yes. Jack Rabbit recalled J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24- per, Order at on 12 Aug 2013. The recall is Class I and its status is Terminated. Recall number D-021-2014.
Why was it recalled?
Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that J.R. Jack Rabbit Male Enhancement product was found to contain two undeclared active pharmaceutical ingredients: sildenafil and tadalafil.
Which lots are affected?
Lot #: 2510 Exp 04/01/15
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 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.