Recall · openFDA Food Enforcement

MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab…: FDA Recall F-0729-2022

Agency action: Oct 6, 2021Record ID: F-0729-2022
View official source ↗

What happened

Original notice title

MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY, recall F-0729-2022

From the archived source record

cGMP Deviations

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Feb 16, 2022
Termination date in the archive
Sep 1, 2022
Source checked
Jul 16, 2026
Record revision
2e8cb03bdd79

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY
Company
ULTRAtab Laboratories, Inc.
Lot / identifier
Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040,19D029, 19D030, 19D031, 19G047, 19G048, 19G049, 19G050
Market / distribution
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.