Goodsense Ultra Strength Antacid Assorted Fruit Tablet, Chewable
FDA Recall NDC 50804-171

FDA Enforcement Report: View Recall Date, Reasons, and Safety Status

Active & Historical Enforcement Reports

The FDA has identified 1 recorded enforcement report(s) associated with Goodsense Ultra Strength Antacid Assorted Fruit (NDC 50804-171). A significant event, classified as Class II, was initiated on May 28, 2026 by Goodsense. The reported reason for this action was: "Presence of foreign substance: small metallic particles in chewable tablets."

This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.

Reported Recall Events

May 2026 Class II Recall: Presence of foreign substance

Recall Number
Class II Ongoing
Reason for Recall
Presence of foreign substance: small metallic particles in chewable tablets.
Initiated
May 28, 2026
Reported
Jun 10, 2026
Quantity
N/A

Recall Profile & Regulatory Data

Event ID
99098
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
Guardian Drug Co. Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
U.S.A. Nationwide
Product Description
GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.
Batch or Lot Expiration Information
Lot# : 1716089, expires: JAN- 2029.
Affected Packages Involved in this Recall
50804-171-68Product

About FDA Recall Enforcement Reports

FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.

If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.