john123131
Well-known member
nice, thanks for the feedback...and man, i live in Canada, cold as hell here, my room I can see my breath..haha...not really, but you'll be ok
ASPIRE36 Reviews thread
- Thread starter Palo Alto Labs
- Start date
im about to order a few bottles of aspire
kaashsindhu
New member
what is the best sexual enhancer for women
ProOne
Member
Scotty, I have some Rhino coming soon....will let you know how it goes
I loved Aspire....
dshiznit00
New member
rhino 51 worked for me it took like 3 hours to kick in but after that it was pretty good
Pseudonymous
New member
ROTFLMAO
I was researching a "porn star stack" on Google, when I came across this thread and was VERY impressed by the rave reviews for Aspire36. Then I found THE FOLLOWING and almost fell out of my chair laughing....
Palo Alto Labs Issues a Voluntary Nationwide Recall of Aspire36 and Aspire Lite, two Products Marketed as Dietary Supplements
FOR IMMEDIATE RELEASE -- Port St. Lucie, FL -- February 28, 2008- Palo Alto Labs, 265 SW Port St. Lucie Blvd., Suite 252, Port St. Lucie, FL 34984, announced today that it is conducting a voluntary nationwide recall of the company's supplement products sold under the name Aspire36 and Aspire Lite. Palo Alto Labs is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Aspire36 and Aspire Lite samples found that the products contained Aildenafil in trace amounts and Dimethyl sildenafil thione (sulfoaildenafil) a purported analog of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED). Sulfoaildenafil is close in structure to Sildenafil and is expected to possess a similar pharmacological and adverse event profile. This may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.
Aspire36 and Aspire Lite are sold nationwide. The products are sold as a blister pack containing one liquid capsule or a bottle containing either three (3) or twelve (12) liquid capsules.
Consumers who have Aspire36 and Aspire Lite in their possession should stop using them immediately. In the event of any adverse side effects due to the consumption of these products, consumers should contact a physician right away. Any adverse events that may be related to the use of these products should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.
The Company is advising consumers to return any unused Aspire36 and Aspire Lite, for a refund of the full purchase price, to the retail location from which it was purchased or to the Company directly if it was purchased from the Company as a part of its Direct Response Program. Consumers can call 1-(877)240-3340 for instructions on the return and refund process.
Palo Alto Labs conducts stringent quality control testing on both raw materials and finished products. Previous testing protocols did not include a test for the presence of Aildenafil or sulfoaildenafil but Palo Alto Labs assures consumers that this deficiency has been rectified. Palo Alto Labs apologizes for any inconvenience and expresses its concern for the health of consumers by conducting a voluntary recall action. Palo Alto Labs promises to ensure quality and integrity of all its products and the company is working closely with the FDA in the recall process.
I was researching a "porn star stack" on Google, when I came across this thread and was VERY impressed by the rave reviews for Aspire36. Then I found THE FOLLOWING and almost fell out of my chair laughing....
Palo Alto Labs Issues a Voluntary Nationwide Recall of Aspire36 and Aspire Lite, two Products Marketed as Dietary Supplements
FOR IMMEDIATE RELEASE -- Port St. Lucie, FL -- February 28, 2008- Palo Alto Labs, 265 SW Port St. Lucie Blvd., Suite 252, Port St. Lucie, FL 34984, announced today that it is conducting a voluntary nationwide recall of the company's supplement products sold under the name Aspire36 and Aspire Lite. Palo Alto Labs is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Aspire36 and Aspire Lite samples found that the products contained Aildenafil in trace amounts and Dimethyl sildenafil thione (sulfoaildenafil) a purported analog of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED). Sulfoaildenafil is close in structure to Sildenafil and is expected to possess a similar pharmacological and adverse event profile. This may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.
Aspire36 and Aspire Lite are sold nationwide. The products are sold as a blister pack containing one liquid capsule or a bottle containing either three (3) or twelve (12) liquid capsules.
Consumers who have Aspire36 and Aspire Lite in their possession should stop using them immediately. In the event of any adverse side effects due to the consumption of these products, consumers should contact a physician right away. Any adverse events that may be related to the use of these products should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.
The Company is advising consumers to return any unused Aspire36 and Aspire Lite, for a refund of the full purchase price, to the retail location from which it was purchased or to the Company directly if it was purchased from the Company as a part of its Direct Response Program. Consumers can call 1-(877)240-3340 for instructions on the return and refund process.
Palo Alto Labs conducts stringent quality control testing on both raw materials and finished products. Previous testing protocols did not include a test for the presence of Aildenafil or sulfoaildenafil but Palo Alto Labs assures consumers that this deficiency has been rectified. Palo Alto Labs apologizes for any inconvenience and expresses its concern for the health of consumers by conducting a voluntary recall action. Palo Alto Labs promises to ensure quality and integrity of all its products and the company is working closely with the FDA in the recall process.
john123131
Well-known member
Wow thanks.....great find....
sarcasm obviously....this was released over a year ago...old news, its no longer produced.
sarcasm obviously....this was released over a year ago...old news, its no longer produced.
john123131
Well-known member
i dont think....im sorry, if its something I can answer i can help you...but im no longer with Palo...
Pseudonymous
New member
Actually it wasn't "obviously sarcasm". This thread didn't mention it. Now that I've posted the info, anyone else who searches for something similar and finds this thread won't be overly impressed by the product (and company) as I was. The relevance of my post is obvious since a few other people are now looking for reps.
john123131
Well-known member
your right im sorry, was sick of seeing it and having a bad day at the time...haha...anyway yes its banned, has been banned now, and they no longer produce it. It was an unknown analogue of the substance at the time. Palo had a recall, and moved on after the final bottles were destroyed. They now have an alternative aspire but clearly is not as potent.
all the best,
bobby