FDA DrugsClass II
GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewabl...
Published: June 10, 2026Recall ID: D-0575-2026Category: drugsCountry: US
Reason for Recall / Hazard
Presence of foreign substance: small metallic particles in chewable tablets.
Product Description & Identification
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.
Additional Source Details
| Field | Value |
|---|---|
| City | Dayton |
| State | NJ |
| Openfda › Unii | H0G9379FGK |
| Openfda › Route | ORAL |
| Openfda › Rxcui | 308892 |
| Openfda › Spl id | 47a791b6-ee4c-49e4-8ba9-b34c55931cb2 |
| Openfda › Brand name | GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT |
| Openfda › Spl set id | ad4d51f6-b55b-45db-b034-fb3da54fbe99 |
| Openfda › Package ndc | 50804-171-68 |
| Openfda › Product ndc | 50804-171 |
| Openfda › Generic name | CALCIUM CARBONATE |
| Openfda › Product type | HUMAN OTC DRUG |
| Openfda › Substance name | CALCIUM CARBONATE |
| Openfda › Manufacturer name | GoodSense |
| Openfda › Application number | M001 |
| Openfda › Is original packager | true |
| Event id | 99098 |
| Address 1 | 2 Charles Ct |
| Code info | Lot #: 1716089, expires: JAN- 2029. |
| Postal code | 08810-1508 |
| Report date | 20260610 |
| Product type | Drugs |
| Reason for recall | Presence of foreign substance: small metallic particles in chewable tablets. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260528 |
| Initial firm notification | Letter |
| Center classification date | 20260603 |
Overview
- Recalling FirmGuardian Drug Co. Inc.
- StatusOngoing
- Risk LevelClass II
- DistributionU.S.A. Nationwide