Arm & Hammer Sodium Bicarbonate Powder Recalled for Contamination
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II. Per the rubric, FDA Class II recalls with potential for significant injury or property damage (such as foreign object contamination) are rated as Severe (4).
Plain-English summary
Church & Dwight Co., Inc. is recalling Arm & Hammer Sodium Bicarbonate Powder, CAS-144-55-8, due to the presence of a foreign substance. The affected product is labeled as USP3 Grade and packaged in bags of various quantities, including 50 lbs. (22.68 kg.) bags. The recall involves a total of 749 tons of the product.
The recall was initiated because the raw material was found to be contaminated with stainless steel and other foreign substances. The affected lots are FF3153, FF3154, FF3155, FF3156, FF3157, and FF3158. The product was distributed nationwide.
Consumers who have purchased this product should check their inventory for the specific lot numbers listed above. If the product is found, it should be returned to the place of purchase or disposed of according to local regulations. The FDA has classified this recall as Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP3 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 469 N. Harrison St., Princeton, NJ 08543-5297; and b) Sodium Bicarbonate U.S.P. No. 3 Fine Powdered, Net Wt. 50 lbs. (22.68 kg.) per
- Manufacturer
- Church & Dwight Inc
- Category
- Drug — Pharmaceutical Excipient
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (6)
- Lot #: FF3153
- FF3154
- FF3155
- FF3156
- FF3157
- and FF3158
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by Church & Dwight Inc under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 5 products in this recall →Related recalls
Same manufacturer · Church & Dwight Inc
See all →- SevereZicam Nasal AllClear swabs recalled over fungal contamination of swabs
FDA (Drugs) · 2025-07-09
- SevereZicam cold remedy nasal swabs recalled over fungal contamination
FDA (Drugs) · 2025-07-09
- SevereOrajel Baby teething swabs recalled over fungal contamination of swabs
FDA (Drugs) · 2025-07-09
- SevereTheraBreath for Kids Oral Rinse Recalled for Yeast Contamination
FDA (Drugs) · 2023-10-25
- HighFirst Response Easy Read App unable to reliably read pregnancy test results
FDA (Devices) · 2023-04-19
Same hazard · foreign substance
See all →- ModerateHeritage Pharmaceuticals Recalls Clindamycin Palmitate Hydrochloride Due to Foreign Particles
FDA (Drugs) · 2026-08-19
- HighPrednisolone Acetate Ophthalmic Suspension Recalled for Foreign Substance
FDA (Drugs) · 2026-07-08
- ModerateCorlanor Ivabradine Tablets Recalled for Foreign Substance Contamination
FDA (Drugs) · 2026-07-01
- LowHydroxyzine Hydrochloride Oral Solution recalled for foreign substance
FDA (Drugs) · 2026-07-01
- ModerateCorlanor ivabradine tablets recalled for presence of foreign substance
FDA (Drugs) · 2026-07-01