ULTRAtab Electrolyte Tablets Recall: Cgmp Deviations Risk
ULTRAtab Laboratories recalls electrolyte tablets due to cGMP deviations. Affected products include specific lots from Highland, NY. Consumers should check product codes and contact the company for details.
Recall notice
cGMP Deviations
Contact the company
What happened, in plain English
ULTRAtab Laboratories is recalling electrolyte tablets that may have manufacturing deviations. This recall is due to cGMP (current good manufacturing practice) issues, which could affect product safety. Read more at govinfonow.com/recall/14044-ultratab-electrolyte-tablets-recall-cgmp-deviations-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/14044-ultratab-electrolyte-tablets-recall-cgmp-deviations-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0722-2022
Cite this page
“ULTRAtab Electrolyte Tablets Recall: Cgmp Deviations Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14044-ultratab-electrolyte-tablets-recall-cgmp-deviations-risk. Based on FDA recall #F-0722-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0722-2022%22&limit=1).
Why it’s dangerous
The recall is for cGMP deviations, which means the manufacturing process did not meet quality standards. This could lead to inconsistent product composition or safety issues, though the exact risk is not specified in the notice.
Who’s affected
Anyone who purchased the affected electrolyte tablets from the listed product codes. People using these tablets for medical purposes or dietary needs are most at risk.
How to tell if you have this one
Check the product codes listed: M693 Bulk Lots 18J001 through 19J046. The tablets contain Calcium 10.8mg, Potassium 40mg, and Magnesium 12mg. They were sold by ULTRAtab Laboratories in Highland, NY.
- Brand
ULTRAtab- Category
Food
All 9 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0721-2022 | Ephrine Plus Tablet (Caffeine 200 mg, Vitamin C 25 mg) Supplement, ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M943 M943L Bulk Lots: 16K038, 18B075 | 4,250,842 tablets |
| F-0722-2022 | Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M693 Bulk Lots: 18J001, 18J002, 18J003, 18L035, 18L036, 18M013, 18M014, 19A044, 19A045, 19B042, 19B043, 19B066, 19C006, 19C007, 19E065, 19E066, 19J045, 19J046 | 26,682,419 tablets |
| F-0723-2022 | Caffeine 125 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M960L Bulk Lots: 19E021, 19E022 | 1,904,760 tablets |
| F-0724-2022 | Caffeine 150 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M961L Bulk Lots: 19E030, 19E031 | 1,606,966 tablets |
| F-0725-2022 | Caffeine 175 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M962L Bulk Lots: 19E032, 19E033 | 1,393,353 tablets |
| F-0726-2022 | Melatonin ER 0.5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M975 Bulk Lots: 19E058 | 955,928 tablets |
| F-0727-2022 | Melatonin ER 2 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M976 Bulk Lots: 19B050, 19F063 | 5,853,539 tablets |
| F-0728-2022 | Melatonin ER 5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M977A Bulk Lots: 19B011, 19B012, 19E023 | 1,478,344 tablets |
| F-0729-2022 | MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY; Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040,19D029, 19D030, 19D031, 19G047, 19G048, 19G049, 19G050 | 42,352,387 tablets |
What to do — step by step
Check Product Codes
Look for the specific product codes listed in the recall notice: M693 Bulk Lots 18J001 through 19J046.
Where it went and when
Where it was distributed
Distributed in Florida and New York.
FDA distribution: “Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, New York.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0722-2022 (October 6, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0722-2022 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.