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RECALL RECORD — CLASS IIRecall closedF-0729-2022/FDA enforcement
Ultratab Laboratories, INC.·Food·Oct 6, 2021

Midnite Tablet (Melatonin 1.5 mg) Supplement, Ultratab Laboratories, INC., Highland, Ny

What you need to know

Class II

  • What happened

    CGMP Deviations

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANY, FLMore food

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Product identification

Source: FDA FOOD

Brand nameUltratab Laboratories, INC.
Recalling firmUltratab Laboratories, INC.Highland, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040, 19D029, 19D030, 19D031, 19G047, 19G048, 19G049, 19G050
Distribution area
NYFL

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

United States

Quantity affected42, 352, 387 tablets
Recall initiationFDA report date: February 16, 2022
FDA recall numberF-0729-2022

Beyond the headline

The recall, in context

Ultratab Laboratories, INC. initiated this food recall on October 6, 2021. The FDA enforcement report states: CGMP Deviations. The FDA report lists distribution as: Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.

The FDA enforcement report describes the reason as: CGMP Deviations

Midnite Tablet (Melatonin 1.5 mg) Supplement, Ultratab Laboratories, INC., Highland, Ny was made or distributed by Ultratab Laboratories, INC. in Highland, NY, United States. This page reflects FDA report F-0729-2022, dated February 16, 2022.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, current good manufacturing practice failures can affect product identity, strength, quality or purity.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Midnite Tablet (Melatonin 1.5 mg) Supplement, Ultratab Laboratories, INC., Highland, Ny recall?

Ultratab Laboratories, INC. recalled Midnite Tablet (Melatonin 1.5 mg) Supplement, Ultratab Laboratories, INC., Highland, Ny in an FDA Class II enforcement action reported as F-0729-2022. CGMP Deviations

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Ultratab Laboratories, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0729-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Ultratab Laboratories, INC.

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Electrolyte Tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), Ultratab Laboratories, …

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Class II·

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Melatonin Er 5 mg Caplet (Supplement), Ultratab Laboratories, INC., Highland, Ny

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.