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Murray International Trading Co., Inc. Recall: Product contains elevated levels of lead and cadmium - F-0275-2022

United States

TerminatedClass II

Company
Murray International Trading Co., Inc.
Product
"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net…
Recall date
November 2, 2021
Terminated
April 30, 2024
Source
FDA

Reason for recall

Product contains elevated levels of lead and cadmium

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz (340g) packaged in a clear plastic box Not published in this source record 13000lbs 16oz Green Plastic Bag Codes: 767533-91001; 767533-91005; 767533-91011; 767533-91018; 767533-91019; 767533-91020; 767533-91049; 767533-91050; 767533-91057; 767533-91060; 767533-91062; 767533-91068; 767533-91070; 767533-91071 12oz Clear Plastic Box Code: 767533-20097

Distribution

  • NY
  • NJ
  • PA
  • MA
  • CT
  • Washington DC
  • VA
  • DE
  • RI
  • FL
  • GA
  • MI
  • IL
  • OH
  • TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0275-2022
Event ID
88974
Status
Terminated
Classification
Class II
Company
Murray International Trading Co., Inc.
Product description
"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz (340g) packaged in a clear plastic box
Quantity
13000lbs
Reason
Product contains elevated levels of lead and cadmium
Recall initiation date
November 2, 2021
Report date
December 8, 2021
Classification date
Not published in this source record
Termination date
April 30, 2024
Distribution pattern
NY, NJ, PA, MA, CT, Washington DC, VA, DE, RI, FL, GA, MI, IL, OH, TX
UPC, lot, and code information
16oz Green Plastic Bag Codes: 767533-91001; 767533-91005; 767533-91011; 767533-91018; 767533-91019; 767533-91020; 767533-91049; 767533-91050; 767533-91057; 767533-91060; 767533-91062; 767533-91068; 767533-91070; 767533-91071 12oz Clear Plastic Box Code: 767533-20097
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Murray International Trading Co., Inc.

Other recalls from Murray International Trading Co., Inc.

FDA Recall TerminatedTerminated: June 14, 2018Historical recordClass II

FUQINGSONG RELIEF CREAM (Flucinonide Ointment), packaged in 50-count individually labeled pieces Net Wt. 0.32oz (10g) within a box, MANUFACTURED BY: TIANJIN MAEDICAL & PHARMACEUTICAL CO., LTD. ADDREST: 96 BAWAEI ROAD, HEDONG COUNTY, TIANJIN CITY, remaining labeling contains Chinese characters.

by Murray International Trading Co., Inc.

Published
July 20, 2016
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 14, 2018Historical recordClass II

Te Xiao BaiNeiTing Herbal Supplement (Naphazoline HCl Solution 0.1%) liquid, Net Wt. 15ml, packaged in a bottle within a box, Produced by: Good Harvests (Asia) Trading Co., Ltd, Imported by Murray Int'l Trading Co., Inc. New York, NY 10013, UPC 7 67533 86115 6, remaining labeling contains Chinese characters.

by Murray International Trading Co., Inc.

Published
July 20, 2016
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 14, 2018Historical recordClass II

PING ON OINTMENT RELIEF FOR MUSCULAR PAIN, packaged in a packet of 12-count 8gm containers within a box, PING ON OINTMENT CO LTD, PING ON OINTMENT INTERNATIONAL LTD, 149 Queen's Road West, Hong Kong, UPC 8 33679 00001 5, remaining labeling contains Chinese characters.

by Murray International Trading Co., Inc.

Published
July 20, 2016
Distribution
Nationwide

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
New York 1
New Jersey 1
Pennsylvania 1
Massachusetts 1
Connecticut 1
District of Columbia 1
Virginia 1
Delaware 1
Rhode Island 1
Florida 1
Georgia 1
Michigan 1
Illinois 1
Ohio 1
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of April 30, 2024.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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