Aphreseller (Ebay seller ID), operating as Buy-herbal.com, announced on Apr. 1 a voluntary nationwide recall of all lots of Kian Pee Wan capsules after U.S. Food and Drug Administration analysis found the presence of undeclared dexamethasone and cyproheptadine in the product.
The recall is significant because these ingredients are not listed on the product label, posing health risks to consumers who may unknowingly ingest prescription drugs. Dexamethasone is a corticosteroid that can impair infection-fighting ability, cause high blood sugar, muscle injuries, psychiatric issues, and cardiovascular events. Prolonged or high-dose use can suppress adrenal gland function with consequences ranging from minor symptoms to death. Sudden discontinuation may also result in withdrawal symptoms. Cyproheptadine is an antihistamine prescribed for allergies; its unlisted presence could lead to side effects such as sedation, dizziness, fatigue, restlessness, dry mouth, gastrointestinal changes, urinary retention, and blurred vision.
Kian Pee Wan capsules are marketed online as a dietary supplement for weight gain and appetite stimulation but are considered an unapproved drug by the FDA due to their undisclosed active pharmaceutical ingredients. The recalled product comes in white bottles with beige labels containing 30 pills each and was distributed nationwide through eBay.com.
Aphreseller said it is notifying customers by press announcement and email while arranging returns for affected products. Customers should stop using Kian Pee Wan capsules immediately and either return them to the place of purchase or dispose of them safely. Those who bought directly from Aphreseller can return items to their Flushing address at 136-61 41st Ave., #602.
Consumers with questions about this recall can contact SiewLee Wong via email at greatremedy68@gmail.com or phone at 347-313-8605 during business hours Monday through Friday. Individuals experiencing health problems related to this product should consult their healthcare provider promptly.
Adverse reactions or quality concerns linked to Kian Pee Wan capsules may be reported directly through the FDA's MedWatch Adverse Event Reporting program online or by mail or fax using forms available on www.fda.gov.
