CLASS III Food recall · Reported 29 Nov 2023 · FDA Enforcement Report
Actiron Dietary Supplement, ActiPharma) ) recalled
ActiPharma is recalling Actiron Dietary Supplement, ActiPharma) ) (, distributed in Puerto Rico. The recall was initiated on 28 Sep 2023 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0463-2024
- FDA event ID
- 93210
- Recalling firm
- ActiPharma, Guaynabo, PR
- Brand
- Actiron
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 28 Sep 2023
- FDA classified
- 17 Nov 2023
- Reported
- 29 Nov 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 28 Sep 2023 | Recall initiated by company | |
| 17 Nov 2023 | Classified by FDA | +50 days |
| 29 Nov 2023 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Product as listed by the FDA
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Where it was distributed
Domestic distribution, in Puerto Rico.
Questions about this recall
Is Actiron Dietary Supplement, ActiPharma) ) ( recalled?
Yes. ActiPharma recalled Actiron Dietary Supplement, ActiPharma) ) ( on 28 Sep 2023. The recall is Class III and its status is Terminated. Recall number F-0463-2024.
Why was it recalled?
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Which lots are affected?
Lot 13309, Exp: 01/26
Where was it sold?
Domestic distribution, in Puerto Rico.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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