CLASS III Food recall · Reported 7 Sep 2016 · FDA Enforcement Report
Sodium Bicarbonate, Cas # 144-55-8, USP/fcc Grade recalled
Natrium Products is recalling Sodium Bicarbonate, Cas # 144-55-8, USP/fcc Grade 1, distributed in Michigan, New Jersey, Rhode Island. The recall was initiated on 27 Jul 2016 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-2005-2016
- FDA event ID
- 74821
- Recalling firm
- Natrium Products, Cortland, NY
- Brand
- Sodium Bicarbonate
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 27 Jul 2016
- FDA classified
- 26 Aug 2016
- Reported
- 7 Sep 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 27 Jul 2016 | Recall initiated by company | |
| 26 Aug 2016 | Classified by FDA | +30 days |
| 7 Sep 2016 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Sodium Bicarbonate bulk lot 08315A may contain varying amounts of lubricating oil (food grade oil designated NSF 11).
Product as listed by the FDA
SODIUM BICARBONATE, CAS # 144-55-8, USP/FCC GRADE 1, NET WEIGHT 50 lbs./22.68 kg --- Natrium Products, Inc. 58 Pendleton Street, Cortland, NY 13045
Where it was distributed
RI, MI, NJ
Questions about this recall
Why was it recalled?
Sodium Bicarbonate bulk lot 08315A may contain varying amounts of lubricating oil (food grade oil designated NSF 11).
Which lots are affected?
Lot 08315A (exp. 8/31/2018)
Where was it sold?
RI, MI, NJ
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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