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Class II · Moderate risk Terminated Initiated Mar 11, 2013 (14 years ago)

BoostYourGrade.com

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Cause type: Unapproved drug

The product was marketed without an approved NDA/ANDA, or does not meet the OTC monograph it claims to follow. Nothing about the product - dose, purity, safety - has been reviewed by FDA, so the claims on the box are unverified. All unapproved drug recalls.

What was recalled

BoostYourGrade.com, Piracetam 390mg Choline 104mg capsules, 250 count bottle, OYC, BoostYourGrade, LLC, Orlando, FL 32826

Recalling firm
Palmer Natural Products
Origin
ID, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-235-2013 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Palmer Natural Products

All 2013 recalls
Class II · Moderate risk

Oxiracetam & Choline

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Terminated Unapproved drug Palmer Natural Products D-236-2013
Class II · Moderate risk

Brain Defogger

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Terminated Unapproved drug Palmer Natural Products D-234-2013
Class II · Moderate risk

Piracetam & Choline

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Terminated Unapproved drug Palmer Natural Products D-233-2013
Class II · Moderate risk

Aniracetam and Choline

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Terminated Unapproved drug Palmer Natural Products D-232-2013

Other unapproved drug recalls from 2013

All unapproved drug recalls
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 50 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. D-1032-2014
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 25 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. D-1031-2014
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 10 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. NDC 10702-010-01 D-1030-2014
Class I · High risk

Virilis Pro

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

Terminated Unapproved drug Haute Health, LLC D-1237-2014