Sisel Recall: FDA Class III

Why it was recalled

Firm is recalling SiselRipt due to the presence of an unapproved artificial sweetener, Cyclamates.

Product description

Sisel, SiselRipt, postWORKOUT, Dietary supplement, net wt 5g (0.17 oz), Internal Company Number F137315-10-01

Lot numbers, UPCs & expiration codes

All products

Where it was sold

nationwide and worldwide to Japan, Slovakia and Australia. No govt/VA/military consignees.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1662-2018
Classification: Class III
Status: Terminated
Recall initiated: Jun 29, 2018
FDA report date: Aug 1, 2018
Quantity: 11,226 (USA)
Recall type: Voluntary: Firm initiated
Recalling firm: Sisel International Llc

Original FDA data

Every field from FDA enforcement report F-1662-2018, exactly as published.

Show all FDA fields

City: Springville
State: UT
Status: Terminated
Country: United States
Event ID: 80398
Address: 1325 W Industrial Cir
Code information: All products
Postal code: 84663-3074
Report date: Aug 1, 2018
Product type: Food
Recall number: F-1662-2018
Classification: Class III
Recalling firm: Sisel International Llc
Product quantity: 11,226 (USA)
Termination date: Nov 13, 2018
Reason for recall: Firm is recalling SiselRipt due to the presence of an unapproved artificial sweetener, Cyclamates.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Sisel, SiselRipt, postWORKOUT, Dietary supplement, net wt 5g (0.17 oz), Internal Company Number F137315-10-01
Distribution pattern: nationwide and worldwide to Japan, Slovakia and Australia. No govt/VA/military consignees.
Recall initiation date: Jun 29, 2018
Initial firm notification: E-Mail
Center classification date: Jul 23, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1662-2018, published Aug 1, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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Sisel Recall

Summary