FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

IQ Formulations E.S.P. Pre-Workout Recall

E.S.P. Pre-Workout, Energy Stimulant Pre-workout, Powder, 300 g, blue raspberry flavor…

IQ Formulations, LLC · Sunrise, FL

Risk level
Class II
Reported by FDA
Feb 1, 2017
Recall ID
F-1347-2017
Check your lot numberHow we source this data

Summary

IQ Formulations recalled E.S.P. Pre-Workout starting Aug 16, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1347-2017 on Feb 1, 2017. Reason: Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients. Status: Terminated.

Why it was recalled

Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients

Product description

E.S.P. Pre-Workout, Energy Stimulant Pre-workout, Powder, 300 g, blue raspberry flavor (UPC 764779-410728.

Lot numbers, UPCs & expiration codes

Lots: 1600807 (Exp 01/11/2019), 1520115 (Exp 12/26/2019), 1603701 (Exp 02/06/2019), 1603702 (Exp 02/06/2019), 1603901 (Exp 02/08/2019), 1603903 (Exp 02/08/2019), 1600806 (Exp 01/11/2019), 1603902 (Exp 02/09/2019), 1604602 (Exp 02/15/2019), 1604601 (Exp 02/15/2019), 1604701 (Exp 02/16/2019), 1604604 (Exp 02/15/2019), 1604603 (Exp 02/15/2019), 1604702 (Exp 02/22/2019), 1604404 (Exp 02/13/2019), 1605601 (Exp 02/25/2019), 1605510 (Exp 02/24/2019), 1605602 (Exp 03/03/2019), 1605509 (Exp 02/24/2019), 1619601 (Exp 07/14/2019), 1619601 (Exp 07/14/2019), 1620401 (Exp 07/22/2019), 1620402 (Exp 07/22/2019), 1620403 (Exp 07/22/2019), 1600708 (Exp 07/08/2019), 1603602 (Exp 02/05/2019), 1603604 (Exp 02/25/2019), 1603603 (Exp 02/05/2019), 1604205 (Exp 02/11/2019), 1604204 (Exp 02/11/2019), 1604203 (Exp 02/11/2019), 1604301 (Exp 02/12/2019), 1604302 (Exp 02/12/2019), 1604303 (Exp 02/12/2019), 1605307 (Exp 02/22/2019), 1605106 (Exp 02/20/2019), 1605105 (Exp 02/20/2019), 1605506 (Exp 02/24/2019), 1605507 (Exp 02/24/2019), 1605508 (Exp 02/24/2019), 1622304 (Exp 08/10/2019), 1603904 (Exp 02/08/2019), 1603905 (Exp 02/08/2019), 1604003 (Exp 02/09/2019), 1604004 (Exp 02/09/2019), 1604005 (Exp 02/09/2019), 1604002 (Exp 02/09/2019), 1604006 (Exp 02/09/2019), 1604806 (Exp 02/17/2019), 1604709 (Exp 02/16/2019), 1604708 (Exp 02/16/2019), 1604903 (Exp 02/18/2019), 1604805 (Exp 02/17/2019), 1604807 (Exp 02/17/2019), 1604003 (Exp 02/09/2019), 1605610 (Exp 02/25/2019), 1604001 (Exp 02/09/2019), 1600707 (Exp 01/09/2019), 1603204 (Exp 02/03/2019), 1603601 (Exp 02/05/2019), 1603509 (Exp 02/04/2019), 1604103 (Exp 02/10/2019), 1604201 (Exp 02/11/2019), 1604101 (Exp 02/10/2019), 1604202 (Exp 02/11/2019), 1604102 (Exp 02/10/2019), 1604104 (Exp 02/10/2019), 1605003 (Exp 02/19/2019), 1605002 (Exp 02/19/2019).1605007 (Exp 02/19/2019), 1604905 (Exp 02/18/2019), 1604906 (Exp 02/18/2019), 1604904 (Exp 02/18/2019), 1605001 (Exp 08/05/2019), 1622303 (Exp 08/10/2019).

Where it was sold

Unknown

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-1347-2017
Classification
Class II
Status
Terminated
Recall initiated
Aug 16, 2016
FDA report date
Feb 1, 2017
Quantity
Approximately 34,100 containers
Recall type
Voluntary: Firm initiated
Recalling firm
IQ Formulations, LLC

Original FDA data

Every field from FDA enforcement report F-1347-2017, exactly as published.

Show all FDA fields
City
Sunrise
State
FL
Status
Terminated
Country
United States
Event ID
75110
Address
523 Sawgrass Corporate Pkwy
Code information
Lots: 1600807 (Exp 01/11/2019), 1520115 (Exp 12/26/2019), 1603701 (Exp 02/06/2019), 1603702 (Exp 02/06/2019), 1603901 (Exp 02/08/2019), 1603903 (Exp 02/08/2019), 1600806 (Exp 01/11/2019), 1603902 (Exp 02/09/2019), 1604602 (Exp 02/15/2019), 1604601 (Exp 02/15/2019), 1604701 (Exp 02/16/2019), 1604604 (Exp 02/15/2019), 1604603 (Exp 02/15/2019), 1604702 (Exp 02/22/2019), 1604404 (Exp 02/13/2019), 1605601 (Exp 02/25/2019), 1605510 (Exp 02/24/2019), 1605602 (Exp 03/03/2019), 1605509 (Exp 02/24/2019), 1619601 (Exp 07/14/2019), 1619601 (Exp 07/14/2019), 1620401 (Exp 07/22/2019), 1620402 (Exp 07/22/2019), 1620403 (Exp 07/22/2019), 1600708 (Exp 07/08/2019), 1603602 (Exp 02/05/2019), 1603604 (Exp 02/25/2019), 1603603 (Exp 02/05/2019), 1604205 (Exp 02/11/2019), 1604204 (Exp 02/11/2019), 1604203 (Exp 02/11/2019), 1604301 (Exp 02/12/2019), 1604302 (Exp 02/12/2019), 1604303 (Exp 02/12/2019), 1605307 (Exp 02/22/2019), 1605106 (Exp 02/20/2019), 1605105 (Exp 02/20/2019), 1605506 (Exp 02/24/2019), 1605507 (Exp 02/24/2019), 1605508 (Exp 02/24/2019), 1622304 (Exp 08/10/2019), 1603904 (Exp 02/08/2019), 1603905 (Exp 02/08/2019), 1604003 (Exp 02/09/2019), 1604004 (Exp 02/09/2019), 1604005 (Exp 02/09/2019), 1604002 (Exp 02/09/2019), 1604006 (Exp 02/09/2019), 1604806 (Exp 02/17/2019), 1604709 (Exp 02/16/2019), 1604708 (Exp 02/16/2019), 1604903 (Exp 02/18/2019), 1604805 (Exp 02/17/2019), 1604807 (Exp 02/17/2019), 1604003 (Exp 02/09/2019), 1605610 (Exp 02/25/2019), 1604001 (Exp 02/09/2019), 1600707 (Exp 01/09/2019), 1603204 (Exp 02/03/2019), 1603601 (Exp 02/05/2019), 1603509 (Exp 02/04/2019), 1604103 (Exp 02/10/2019), 1604201 (Exp 02/11/2019), 1604101 (Exp 02/10/2019), 1604202 (Exp 02/11/2019), 1604102 (Exp 02/10/2019), 1604104 (Exp 02/10/2019), 1605003 (Exp 02/19/2019), 1605002 (Exp 02/19/2019).1605007 (Exp 02/19/2019), 1604905 (Exp 02/18/2019), 1604906 (Exp 02/18/2019), 1604904 (Exp 02/18/2019), 1605001 (Exp 08/05/2019), 1622303 (Exp 08/10/2019).
Postal code
33325-6259
Report date
Feb 1, 2017
Product type
Food
Recall number
F-1347-2017
Classification
Class II
Recalling firm
IQ Formulations, LLC
Product quantity
Approximately 34,100 containers
Termination date
Sep 20, 2024
Reason for recall
Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients
Voluntary / mandated
Voluntary: Firm initiated
Product description
E.S.P. Pre-Workout, Energy Stimulant Pre-workout, Powder, 300 g, blue raspberry flavor (UPC 764779-410728.
Distribution pattern
Unknown
Recall initiation date
Aug 16, 2016
Initial firm notification
E-Mail
Center classification date
Jan 25, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1347-2017, published Feb 1, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls