HIGHFDA DRUG

HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.

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

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
May 28, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 28, 2026
Hazard Level
HIGH
Brand
Guardian Drug Co.
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Guardian Drug Co.
Model numbers
Lot #: 1276119, expires: Jan 2029.
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 28, 2026

  2. Reported by FDA DRUG

    June 10, 2026

  3. RecallRadar source check

    June 16, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Guardian Drug Co. Inc. or your healthcare provider for guidance. Notification method: Letter

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Full Description

HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.. Reason: Presence of foreign substance: small metallic particles in chewable tablets.. Classification: Class II. Distribution: U.S.A. Nationwide

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot #: 1276119
expires: Jan 2029.
Affected States
ALL
Report Date
June 10, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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