CLASS II Food recall · Reported 16 Feb 2022 · FDA Enforcement Report
Electrolyte tablet (Calcium 10.8mg, Potassium 40mg recalled
ULTRAtab Laboratories is recalling Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab, distributed in Florida, New York. The recall was initiated on 6 Oct 2021 and the FDA has classified it as Class II.
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-0722-2022
- FDA event ID
- 89512
- Recalling firm
- ULTRAtab Laboratories, Highland, NY
- Brand
- Electrolyte
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Oct 2021
- FDA classified
- 9 Feb 2022
- Reported
- 16 Feb 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Energy Drinks
Timeline
| 6 Oct 2021 | Recall initiated by company | |
| 9 Feb 2022 | Classified by FDA | +126 days |
| 16 Feb 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
cGMP Deviations
Product as listed by the FDA
Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab Laboratories, Inc., Highland, NY
Where it was distributed
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Questions about this recall
Why was it recalled?
cGMP Deviations
Which lots are affected?
Product Codes: M693 Bulk Lots: 18J001, 18J002, 18J003, 18L035, 18L036, 18M013, 18M014, 19A044, 19A045, 19B042, 19B043, 19B066, 19C006, 19C007, 19E065, 19E066, 19J045, 19J046
Where was it sold?
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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.
Other products in this recall event
8 other products · FDA event 89512More recalls from ULTRAtab Laboratories
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