FDAClass IIJune 10, 2026

EQUALINE ultra strength recall

EQUALINE ultra strength, antacid tablets, calcium carbonate 1000mg, 72 chewable tablets, DISTRIBUTED BY SUPERVALU INC.,EDEN PRARIE, MN 55344 USA, NDC 41163-171-68.

Why was EQUALINE ultra strength recalled?

Presence of foreign substance: small metallic particles in chewable tablets.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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 #: 1716089, expires: JAN- 2029.

Product
EQUALINE ultra strength, antacid tablets, calcium carbonate 1000mg, 72 chewable tablets, DISTRIBUTED BY SUPERVALU INC.,EDEN PRARIE, MN 55344 USA, NDC 41163-171-68.
Recalling firm
Guardian Drug Co. Inc.
Distribution
U.S.A. Nationwide
Recall date
June 10, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (drug)
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