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Class I: serious health riskTerminated

ABH Nature's Products Arthri-D 120ct Recall

Arthri-D 120ct

ABH Nature's Products, Inc. · Edgewood, NY

Risk level
Class I
Reported by FDA
Feb 21, 2018
Recall ID
F-0812-2018
Check your lot numberHow we source this data

Summary

ABH Nature's Products recalled Arthri-D 120ct starting Jan 20, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-0812-2018 on Feb 21, 2018. Reason: Product may be contaminated with Salmonella. Status: Terminated.

Why it was recalled

Product may be contaminated with Salmonella.

Product description

Arthri-D 120ct

Lot numbers, UPCs & expiration codes

Lot# 1701-092

Where it was sold

Direct to MA and PA

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-0812-2018
Classification
Class I
Status
Terminated
Recall initiated
Jan 20, 2018
FDA report date
Feb 21, 2018
Quantity
10,100 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
ABH Nature's Products, Inc.

Original FDA data

Every field from FDA enforcement report F-0812-2018, exactly as published.

Show all FDA fields
City
Edgewood
State
NY
Status
Terminated
Country
United States
Event ID
78983
Address
131 Heartland Blvd
Code information
Lot# 1701-092
Postal code
11717-8315
Report date
Feb 21, 2018
Product type
Food
Recall number
F-0812-2018
Classification
Class I
Recalling firm
ABH Nature's Products, Inc.
Product quantity
10,100 bottles
Termination date
Jun 19, 2018
Reason for recall
Product may be contaminated with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Arthri-D 120ct
Distribution pattern
Direct to MA and PA
Recall initiation date
Jan 20, 2018
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 15, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0812-2018, published Feb 21, 2018. View the source record (openFDA) · FDA enforcement reports

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

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