Ferrous Sulfate 325 MG tablet recall
Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
Why was Ferrous Sulfate 325 MG tablet recalled?
Presence of Foreign Tablets/Capsules
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?
NDC 33261-0715-00 Batch ID: 57909-1, exp. date 04/30/2019 57909-2, exp. date 06/30/2019
- Product
- Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
- Recalling firm
- Aidarex Pharmaceuticals LLC
- Quantity
- 450 bottles
- Distribution
- Product was distributed to Florida
- Recall date
- May 23, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)