FDAClass IIRecall started June 11, 2013

Sodium Bicarbonate Powder (D-800-2013) Recall: Contamination

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…

What is the FDA recall status?

The FDA record lists this recall as terminated. This does not establish that a retained recalled product is safe to consume or use. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions.

How FDA enforcement data reports status

Why was Sodium Bicarbonate Powder recalled?

Presence of Foreign Substance: raw material recalled due to stainless steel and other contamination.

What should I do if I have this product?

Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.

Full product description

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.

Which lot codes, UPCs or models are affected?

Lot #: FF3153, FF3154, FF3155, FF3156, FF3157, and FF3158

Agency record number
D-800-2013
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…
Recalling firm
Church & Dwight Inc
Quantity
749 tons total
Distribution
Nationwide
Recall started
June 11, 2013
Report date
July 24, 2013
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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