Arm & Hammer Sodium Bicarbonate Powder Recalled for Foreign Substance Contamination
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II and involves a risk-of-harm product (foreign substance contamination) where no specific injuries or illnesses have been reported in the source text, fitting the 'High' severity criteria for theoretical or unreported harm risks.
Plain-English summary
Church & Dwight Inc. is recalling Arm & Hammer Sodium Bicarbonate Powder, labeled as USP2 Grade or Sodium Bicarbonate U.S.P. No. 2 Fine Granular, due to the presence of a foreign substance. The raw material was found to be contaminated with stainless steel and other materials.
The recall involves 749 tons of the product, distributed nationwide. The affected lots are FF3153, FF3154, FF3155, FF3156, FF3157, and FF3158. The product is packaged in bags of various quantities, including 50 lbs. (22.68 kg.) bags.
Consumers who have purchased this product should stop using it and contact Church & Dwight Inc. for further instructions. The FDA has classified this recall as Class II, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP2 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. 2 Fine Granular, 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
Similar recalls
- ModerateArm & Hammer Baking Soda Recalled for Metal Contamination
FDA (Food) · 2013-08-07
- HighChurch & Dwight Recalls Contaminated Sodium Bicarbonate for Medical Use
FDA (Devices) · 2013-07-31
- SevereSodium Bicarbonate Injection recalled due to glass contamination
FDA (Drugs) · 2023-11-15
- ModerateNatrium Products Recalls Sodium Bicarbonate Due to Lubricating Oil Contamination
FDA (Food) · 2016-09-07
- SevereSodium Bicarbonate Injection recalled for glass particulate contamination
FDA (Drugs) · 2024-01-24
- ModerateB&B Pharmaceuticals Recalls Estradiol Powder Due to Foreign Material
FDA (Drugs) · 2020-04-22