ACTIRON Dietary Supplement recall
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Why was ACTIRON Dietary Supplement 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 13309, Exp: 01/26
- Product
- ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
- Recalling firm
- ActiPharma, Inc.
- Quantity
- 607 bottles of 100 tablets each
- Distribution
- Domestic distribution, in Puerto Rico.
- Recall date
- November 29, 2023
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (food)