Dietary supplement

Hydro Pineapple Burn food supplement recalled due to undeclared sibutramine | WGN 720 radio

Hydro Pineapple Burn (FDA image)

The FDA has published the following:

Houston, Texas, eBay Seller ID: jongu 4308 is voluntarily recalling all batches of Hydro Pineapple Burn at the consumer level. An FDA analysis found the product to contain undeclared sibutramine. Sibutramine was an FDA approved drug used as an appetite suppressant for weight loss, but was taken off the market due to safety concerns. The presence of sibutramine in Hydro Pineapple Burn makes it an unapproved drug for which the safety and effectiveness have not been established and therefore subject to recall. To date, jongu 4308 has not received any reports of adverse events related to this recall.

Risk Statement: Products containing sibutramine pose a risk to the health of consumers because sibutramine is known to dramatically increase blood pressure and / or pulse in some patients and may pose a significant risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmia or stroke.

This spoiled product is marketed as a dietary supplement for weight loss and is packaged in a box containing ten sachets of 20g. Hydro Pineapple Burn was distributed by eBay via the Internet at www.ebay.com nationwide in the United States (05/29/2021 to 07/27/2021). On August 3, 2021, the FDA issued a press release warning consumers to avoid certain products found on eBay, Amazon, and other retailers due to hidden and potentially dangerous drug ingredients. He also encouraged online marketplaces to ensure that these products are not sold on their platforms.

EBay Seller ID: jongu 4308 is informing its customers through this press release and by email of this recall. Consumers who have the recalled Hydro Pineapple Burn should stop using them and destroy them. Consumers with questions regarding this recall can contact eBay seller number: jongu 4308 by sending a message on eBbay or by email: [email protected] Consumers should contact their doctor or health care provider if they have had any problems that may be related to taking or using this medication.

Adverse reactions or quality issues encountered while using this product can be reported to the MedWatch Adverse Event Reporting Program of the FDA, either online, by regular mail, or by fax.

  • Complete and submit the report online
  • Regular Mail or Fax: Download the form or call 1-800-332-1088 to request a report form, then complete and return it to the address on the pre-addressed form, or fax it to 1-800-FDA-0178

This recall is being made with the knowledge of the United States Food and Drug Administration.


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