Sodium Bicarbonate Powder — Class II drug recall D-800-2013
Terminated recall by Church & Dwight Inc, reported 2013-07-24, distributed nationwide. Presence of Foreign Substance: raw material recalled due to stainless steel and other contamination.
| Recall number | D-800-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Inc, Princeton, NJ, United States |
| Recall initiated | 2013-06-11 |
| Classified | 2013-07-12 |
| Reported by FDA | 2013-07-24 |
| Terminated | 2015-06-30 |
| Distributed | Nationwide (US) |
| Quantity | 749 tons |
| Lot numbers | FF3153, FF3154, FF3155, FF3156, FF3157, FF3158 |
Product
Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, Sodium Bicarbonate U.S.P. No. 4 Granular, Net Wt. 50 lbs. (22.68 kg.) per bag, Manufactured by: Church & Dwight Co., Inc., 469 N. Harrison St., Princeton, N.J. 08543-5297, Product #60411.
Reason for recall
Presence of Foreign Substance: raw material recalled due to stainless steel and other contamination.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-800-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.