US Food Recall Atlas

A single recall record, as the agency published it.

Recall mapAll recalls → F-0729-2022

MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY ULTRAtab Laboratories, Inc. · reported 2022-02-16

Terminated This recall has been closed out by the agency.

Reason for recall
cGMP Deviations
Classification
Class II
Recall initiated
2021-10-06
Reported by the agency
2022-02-16
Closed out (terminated)
2022-09-01
Recalling firm
ULTRAtab Laboratories, Inc.
Highland, NY
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
States we parsed from that text
FL NY

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
Dietary supplementsderived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-0729-2022

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.