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Class II: temporary or reversible health riskTerminated

ULTRAtab Laboratories Electrolyte tablet Recall

Electrolyte tablet (Calcium 10

ULTRAtab Laboratories, Inc. · Highland, NY

Risk level
Class II
Reported by FDA
Feb 16, 2022
Recall ID
F-0722-2022
Check your lot numberHow we source this data

Summary

ULTRAtab Laboratories recalled Electrolyte tablet starting Oct 6, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0722-2022 on Feb 16, 2022. Reason: cGMP Deviations. Status: Terminated.

Why it was recalled

cGMP Deviations

Product description

Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab Laboratories, Inc., Highland, NY

Lot numbers, UPCs & expiration codes

Product Codes: M693 Bulk Lots: 18J001, 18J002, 18J003, 18L035, 18L036, 18M013, 18M014, 19A044, 19A045, 19B042, 19B043, 19B066, 19C006, 19C007, 19E065, 19E066, 19J045, 19J046

Where it was sold

Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0722-2022
Classification
Class II
Status
Terminated
Recall initiated
Oct 6, 2021
FDA report date
Feb 16, 2022
Quantity
26,682,419 tablets
Recall type
Voluntary: Firm initiated
Recalling firm
ULTRAtab Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report F-0722-2022, exactly as published.

Show all FDA fields
City
Highland
State
NY
Status
Terminated
Country
United States
Event ID
89512
Address
50 Toc Dr
Code information
Product Codes: M693 Bulk Lots: 18J001, 18J002, 18J003, 18L035, 18L036, 18M013, 18M014, 19A044, 19A045, 19B042, 19B043, 19B066, 19C006, 19C007, 19E065, 19E066, 19J045, 19J046
Postal code
12528-1506
Report date
Feb 16, 2022
Product type
Food
Recall number
F-0722-2022
Classification
Class II
Recalling firm
ULTRAtab Laboratories, Inc.
Product quantity
26,682,419 tablets
Termination date
Sep 1, 2022
Reason for recall
cGMP Deviations
Voluntary / mandated
Voluntary: Firm initiated
Product description
Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab Laboratories, Inc., Highland, NY
Distribution pattern
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Recall initiation date
Oct 6, 2021
Initial firm notification
Letter
Center classification date
Feb 9, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0722-2022, published Feb 16, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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