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Class III: unlikely to cause harmTerminated

Infiniti Creations Natural Protocols Recall

Natural Protocols

Infiniti Creations, LLC · Lindon, UT

Risk level
Class III
Reported by FDA
Nov 30, 2016
Recall ID
F-0484-2017
Check your lot numberHow we source this data

Summary

Infiniti Creations recalled Natural Protocols starting Sep 30, 2016. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0484-2017 on Nov 30, 2016. Reason: The firm announced a voluntary recall of various dietary supplement products due to misbranding and some products may contain undeclared HCG. Status: Terminated.

Why it was recalled

The firm announced a voluntary recall of various dietary supplement products due to misbranding and some products may contain undeclared HCG.

Product description

Natural Protocols. 2oz HCG Drops. Amber Glass

Lot numbers, UPCs & expiration codes

Lots: HC0815B; IC1215L-MW

Where it was sold

Nationwide and Canada. No other foreign and military/govt/VA 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-0484-2017
Classification
Class III
Status
Terminated
Recall initiated
Sep 30, 2016
FDA report date
Nov 30, 2016
Quantity
40 units
Recall type
Voluntary: Firm initiated
Recalling firm
Infiniti Creations, LLC

Original FDA data

Every field from FDA enforcement report F-0484-2017, exactly as published.

Show all FDA fields
City
Lindon
State
UT
Status
Terminated
Country
United States
Event ID
75342
Address
1453 W 40 S
Code information
Lots: HC0815B; IC1215L-MW
Postal code
84042-1626
Report date
Nov 30, 2016
Product type
Food
Recall number
F-0484-2017
Classification
Class III
Recalling firm
Infiniti Creations, LLC
Product quantity
40 units
Termination date
Mar 31, 2017
Reason for recall
The firm announced a voluntary recall of various dietary supplement products due to misbranding and some products may contain undeclared HCG.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Natural Protocols. 2oz HCG Drops. Amber Glass
Distribution pattern
Nationwide and Canada. No other foreign and military/govt/VA consignees.
Recall initiation date
Sep 30, 2016
Initial firm notification
Letter
Center classification date
Nov 22, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0484-2017, published Nov 30, 2016. View the source record (openFDA) · FDA enforcement reports

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

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