Key Takeaway

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00 by Aidarex Pharmaceuticals LLC was recalled on April 10, 2018. The hazard: Presence of Foreign Tablets/Capsules

FDA Drug Class III Terminated

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00

Recalled: April 10, 2018 ~450 bottles units affected D-0810-2018

Description

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00

Hazard / Reason

Presence of Foreign Tablets/Capsules

Class III: Product that is not likely to cause adverse health consequences.

Class III is the least severe classification. The product is unlikely to cause adverse health consequences but still violates FDA regulations.

Products Affected

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00

Drugs

Company Information

Aidarex Pharmaceuticals LLC

Corona, CA, United States

View all 10 recalls by Aidarex Pharmaceuticals LLC →

Distribution

Product was distributed to Florida

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Frequently Asked Questions

Is this recall still active?

Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.

How do I check if my product is affected?

Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

Check the remedy section above or contact the manufacturer directly for current remedy options.

Where can I find the original recall notice?

This recall was issued by FDA Drug. Visit the agency's official website for the original notice.

Data sourced from FDA Drug Enforcement. Recall information may not reflect the most current status. RecallDex is not affiliated with any US government agency. Contact the manufacturer or relevant agency for the latest information.