Recall events
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Event 64619
Event summary
Timeline bucket March 11, 2013
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Palmer Natural Products
Dossier provenance
Source snapshots represented here
openFDA Drug Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
7 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
drug · product 1 of 7
Aniracetam & Choline capsules, 430mg Aniracetam 88mg Choline, a) 30 count bottle b) 60 count bottle, c) 90 count, d) 180 count , OTC, BoostYourGrade, LLC Orlando, FL 32826
D-230-2013
Recall number D-230-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 557 30 count botles, 672 60 count bottles, 1,102 90 count bottles, 250 180 count bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes.
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8400]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 7
NOOTROPA COGNITIVE ENHANCEMENT SUPPLEMENT, 400 mg Aniracetam Capsules 60 count bottle, OTC Manufactured & Packaged in the USA for NOOTROPA.COM. DEVELOPED BY: Digital Superfuture Limited Arntel Building 9B 148 Des Voeux Rd. Hong Kong.
D-231-2013
Recall number D-231-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 672 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information Lot HJLA,
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8402]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 7
Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg, 180 capsules per bottler, non-Rx, distributed by BoostYourGrade, BoostYourGrade, LLC Orlando, FL
D-232-2013
Recall number D-232-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 250 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes.
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[5626]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 7
Piracetam & Choline, 390mg Piracetam 104mg Choline Capsules, a) 30 count bottle, b) 100 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. 32826 ,
D-233-2013
Recall number D-233-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 511 30 count bottles, 4103 100 count bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes.
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[5586]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 7
Brain Defogger, Piracetam 390mg Choline 104mg capsules, 100 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. .
D-234-2013
Recall number D-234-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 4103 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes.
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[5623]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 7
BoostYourGrade.com, Piracetam 390mg Choline 104mg capsules, 250 count bottle, OYC, BoostYourGrade, LLC, Orlando, FL 32826
D-235-2013
Recall number D-235-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 723 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes.
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[5672]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 7
Oxiracetam & Choline , Oxiracetam 460mg Choline 110mg capsules a) 30 count bottle, b) 60 count bottle, c) 90 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. 32826
D-236-2013
Recall number D-236-2013
Initiated March 11, 2013
Classification Class II
Status Terminated
Quantity 472 - 30 count bottles; 203 - 60 count bottles; 458 - 90 count bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Code information All lot codes
Distribution pattern Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[7169]
FDA event record
· Exact recall-number query on openFDA
